Small supernumerary marker chromosome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Small supernumerary marker chromosome" in English language version.

refsWebsite

Global rank English rank

76nih.gov

4^th place

45doi.org

2^nd place

11semanticscholar.org

11^th place

8^th place

2harvard.edu

18^th place

17^th place

2omim.org

4,380^th place

4,305^th place

1mun-h-center.se

low place

1medlineplus.gov

1,581^st place

1,299^th place

1orpha.net

3,537^th place

7,177^th place

1cardiff.ac.uk

low place

7,039^th place

cardiff.ac.uk

orca.cardiff.ac.uk

Davies W (April 2021). "The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes" (PDF). European Journal of Medical Genetics. 64 (4): 104169. doi:10.1016/j.ejmg.2021.104169. PMID 33610733. S2CID 231987679.

doi.org

Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T (February 2016). "Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors". Molecular Syndromology. 6 (5): 210–21. doi:10.1159/000441408. PMC 4772618. PMID 26997941.
Reddy KS, Aradhya S, Meck J, Tiller G, Abboy S, Bass H (January 2013). "A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity". Genetics in Medicine. 15 (1): 3–13. doi:10.1038/gim.2012.78. PMID 22935720.
Slimani W, Jelloul A, Al-Rikabi A, Sallem A, Hasni Y, Chachia S, Ernez A, Chaieb A, Bibi M, Liehr T, Saad A, Mougou-Zerelli S (July 2020). "Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives". Journal of Assisted Reproduction and Genetics. 37 (7): 1729–1736. doi:10.1007/s10815-020-01811-9. PMC 7376793. PMID 32399795.
Lu Y, Liang Y, Ning S, Deng G, Xie Y, Song J, Zuo N, Feng C, Qin Y (2020). "Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder". Molecular Cytogenetics. 13: 21. doi:10.1186/s13039-020-00489-z. PMC 7288499. PMID 32536972.
Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S (September 2017). "Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization". Scientific Reports. 7 (1): 10395. Bibcode:2017NatSR...710395S. doi:10.1038/s41598-017-10466-z. PMC 5583289. PMID 28871159.
Liehr T, Al-Rikabi A (2019). "Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review". Frontiers in Genetics. 10: 1131. doi:10.3389/fgene.2019.01131. PMC 6859531. PMID 31781176.
Matsubara K, Yanagida K, Nagai T, Kagami M, Fukami M (2020). "De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue". Frontiers in Genetics. 11: 132. doi:10.3389/fgene.2020.00132. PMC 7056893. PMID 32174976.
Olszewska M, Wanowska E, Kishore A, Huleyuk N, Georgiadis AP, Yatsenko AN, Mikula M, Zastavna D, Wiland E, Kurpisz M (November 2015). "Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient". Scientific Reports. 5: 17408. Bibcode:2015NatSR...517408O. doi:10.1038/srep17408. PMC 4663790. PMID 26616419.
He X, Pang Z, Zhang X, Lan T, Chen H, Chen M, Yang H, Huang J, Chen Y, Zhang Z, Jing W, Peng R, Zhang H (September 2018). "Consistent Amplification of FRS2 and MDM2 in Low-grade Osteosarcoma: A Genetic Study of 22 Cases With Clinicopathologic Analysis". The American Journal of Surgical Pathology. 42 (9): 1143–1155. doi:10.1097/PAS.0000000000001125. PMID 30001240. S2CID 51618887.
Kang JY, Kim HJ, Wojno TH, Yeung AM, Mendoza PR, Grossniklaus HE (2021). "Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma of the Orbit: Three Cases and Review of the Literature". Ophthalmic Plastic and Reconstructive Surgery. 37 (3S): S134–S140. doi:10.1097/IOP.0000000000001804. PMID 32991496. S2CID 222143763.
Huang XL, de Michelena MI, Mark H, Harston R, Benke PJ, Price SJ, Milunsky A (December 2005). "Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses". Clinical Genetics. 68 (6): 513–9. doi:10.1111/j.1399-0004.2005.00523.x. PMID 16283881. S2CID 11293671.
Chen CP, Ko TM, Chen YY, Su JW, Wang W (September 2013). "Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome". Gene. 527 (1): 384–8. doi:10.1016/j.gene.2013.05.061. PMID 23747353.
Xue H, Chen X, Lin M, Lin N, Huang H, Yu A, Xu L (December 2020). "Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis". Aging. 13 (2): 2135–2148. doi:10.18632/aging.202220. PMC 7880375. PMID 33318309.
Knijnenburg J, van Bever Y, Hulsman LO, van Kempen CA, Bolman GM, van Loon RL, Beverloo HB, van Zutven LJ (September 2012). "A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family". European Journal of Human Genetics. 20 (9): 986–9. doi:10.1038/ejhg.2012.43. PMC 3421127. PMID 22395867.
Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W (July 2020). "Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)". Taiwanese Journal of Obstetrics & Gynecology. 59 (4): 580–585. doi:10.1016/j.tjog.2020.05.019. PMID 32653133.
Xu H, Xiao B, Ji X, Hu Q, Chen Y, Qiu W (July 2014). "Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature". European Journal of Medical Genetics. 57 (7): 329–33. doi:10.1016/j.ejmg.2014.04.011. PMID 24793337.
George-Abraham JK, Zimmerman SL, Hinton RB, Marino BS, Witte DP, Hopkin RJ (August 2012). "Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation". American Journal of Medical Genetics. Part A. 158A (8): 1971–6. doi:10.1002/ajmg.a.35428. PMID 22711292. S2CID 22007065.
Luo Y, Lin J, Sun Y, Qian Y, Wang L, Chen M, Dong M, Jin F (2020). "Non-invasive prenatal screening for Emanuel syndrome". Molecular Cytogenetics. 13: 9. doi:10.1186/s13039-020-0476-7. PMC 7057502. PMID 32158503.
Vinkšel M, Volk M, Peterlin B, Lovrecic L (June 2019). "A Systematic Clinical Review of Prenatally Diagnosed Tetrasomy 9p". Balkan Journal of Medical Genetics. 22 (1): 11–20. doi:10.2478/bjmg-2019-0012. PMC 6714344. PMID 31523615.
Bellil H, Herve B, Herzog E, Ayoubi JM, Vialard F, Poulain M (March 2020). "A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report". Journal of Assisted Reproduction and Genetics. 37 (3): 573–577. doi:10.1007/s10815-020-01690-0. PMC 7125280. PMID 31981038.
Roulet-Coudrier F, Rouibi A, Thuillier C, Bourthoumieu S, Lebbar A, Dupont JM, Yardin C (February 2015). "Unusual isochromosome 5p marker chromosome". American Journal of Medical Genetics. Part A. 167A (2): 455–9. doi:10.1002/ajmg.a.36843. PMID 25424187. S2CID 33445674.
Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB (January 2020). "Diagnosis and clinical delineation of mosaic tetrasomy 5p". European Journal of Medical Genetics. 63 (1): 103634. doi:10.1016/j.ejmg.2019.02.006. PMID 30797979. S2CID 73476547.
Tesner P, Drabova J, Stolfa M, Kudr M, Kyncl M, Moslerova V, Novotna D, Kremlikova Pourova R, Kocarek E, Rasplickova T, Sedlacek Z, Vlckova M (2018). "A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature". Molecular Cytogenetics. 11: 29. doi:10.1186/s13039-018-0377-1. PMC 5941596. PMID 29760779.
Bawazeer S, Alshalan M, Alkhaldi A, AlAtwi N, AlBalwi M, Alswaid A, Alfadhel M (2018). "Tetrasomy 18p: case report and review of literature". The Application of Clinical Genetics. 11: 9–14. doi:10.2147/TACG.S153469. PMC 5811181. PMID 29467581.
Rydzanicz M, Olszewski P, Kedra D, Davies H, Filipowicz N, Bruhn-Olszewska B, Cavalli M, Szczałuba K, Młynek M, Machnicki MM, Stawiński P, Kostrzewa G, Krajewski P, Śladowski D, Chrzanowska K, Dumanski JP, Płoski R (January 2021). "Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications". Molecular Genetics & Genomic Medicine. 9 (1): e1526. doi:10.1002/mgg3.1526. PMC 7963419. PMID 33319479.
Arghir A, Popescu R, Resmerita I, Budisteanu M, Butnariu LI, Gorduza EV, Gramescu M, Panzaru MC, Papuc SM, Sireteanu A, Tutulan-Cunita A, Rusu C (May 2021). "Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review". Genes. 12 (6): 811. doi:10.3390/genes12060811. PMC 8226674. PMID 34073526.
Davies W (April 2021). "The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes" (PDF). European Journal of Medical Genetics. 64 (4): 104169. doi:10.1016/j.ejmg.2021.104169. PMID 33610733. S2CID 231987679.
Wang H, Wang T, Yang N, He Y, Chen L, Hong L, Shao X, Li H, Zhu H, Li H (June 2017). "The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype". Oncology Letters. 13 (6): 4385–4389. doi:10.3892/ol.2017.5965. PMC 5452876. PMID 28588710.
Armanet N, Tosca L, Brisset S, Liehr T, Tachdjian G (2015). "Small Supernumerary Marker Chromosomes in Human Infertility". Cytogenetic and Genome Research. 146 (2): 100–8. doi:10.1159/000438718. PMID 26398339.
Sun M, Zhang H, Xi Q, Li L, Hu X, Zhang H, Liu R (October 2020). "Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems: Three case reports and literature review". Medicine. 99 (40): e22532. doi:10.1097/MD.0000000000022532. PMC 7535553. PMID 33019458.
Pei J, Flieder DB, Talarchek JN, Cooper HS, Patchefsky AS, Wei S (March 2021). "Clinical Application of Chromosome Microarray Analysis in the Diagnosis of Lipomatous Tumors". Applied Immunohistochemistry & Molecular Morphology. 29 (8): 592–598. doi:10.1097/PAI.0000000000000923. PMID 33734108. S2CID 232299293.
Usuda D, Takeshima K, Sangen R, Nakamura K, Hayashi K, Okamura H, Kawai Y, Kasamaki Y, Iinuma Y, Saito H, Kanda T, Urashima S (October 2018). "Atypical lipomatous tumor in the ligamentum teres of liver: A case report and review of the literature". World Journal of Clinical Cases. 6 (12): 548–553. doi:10.12998/wjcc.v6.i12.548. PMC 6212614. PMID 30397612.
Nishio J, Iwasaki H, Shibata T, Nabeshima K, Naito M (April 2016). "Duplication of chromosome segment 12q13–15 in a lipomatous tumor with minimal nuclear atypia: A case report". Oncology Letters. 11 (4): 2875–2878. doi:10.3892/ol.2016.4305. PMC 4812505. PMID 27073568.
Macchia G, Severgnini M, Purgato S, Tolomeo D, Casciaro H, Cifola I, L'Abbate A, Loverro A, Palumbo O, Carella M, Bianchini L, Perini G, De Bellis G, Mertens F, Rocchi M, Storlazzi CT (March 2018). "The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer". Genetics. 208 (3): 951–961. doi:10.1534/genetics.117.300552. PMC 5844343. PMID 29279323.
Bielack SS, Hecker-Nolting S, Blattmann C, Kager L (2016). "Advances in the management of osteosarcoma". F1000Research. 5: 2767. doi:10.12688/f1000research.9465.1. PMC 5130082. PMID 27990273.
Forus A, Bjerkehagen B, Sirvent N, Meza-Zepeda LA, Coindre JM, Berner JM, Myklebost O, Pedeutour F (November 2001). "A well-differentiated liposarcoma with a new type of chromosome 12-derived markers". Cancer Genetics and Cytogenetics. 131 (1): 13–8. doi:10.1016/s0165-4608(01)00516-7. PMID 11734312.
Morin JP, Saltzman AF (May 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.
Chen J, Guo M, Luo M, Deng S, Tian Q (April 2021). "Clinical characteristics and management of Turner patients with a small supernumerary marker chromosome". Gynecological Endocrinology. 37 (8): 730–734. doi:10.1080/09513590.2021.1911992. PMID 33870841. S2CID 233298107.
Barros BA, Moraes SG, Coeli FB, Assumpção JG, De Mello MP, Maciel-Guerra AT, Carvalho AB, Viguetti-Campos N, Vieira TA, Amstalden EM, Andrade JG, Esquiaveto-Aun AM, Marques-de-Faria AP, D'Souza-Li LF, Lemos-Marini SH, Guerra G (December 2011). "OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences". Human Reproduction (Oxford, England). 26 (12): 3450–5. doi:10.1093/humrep/der310. PMID 21930534.
Röthlisberger B, Zerova T, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A (December 2001). "Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child". Journal of Medical Genetics. 38 (12): 885–8. doi:10.1136/jmg.38.12.885. PMC 1734780. PMID 11768396.
Fadl-Elmula I (August 2005). "Chromosomal changes in uroepithelial carcinomas". Cell & Chromosome. 4: 1. doi:10.1186/1475-9268-4-1. PMC 1199610. PMID 16083510.
Atkin NB (May 1997). "Cytogenetics of carcinoma of the cervix uteri: a review". Cancer Genetics and Cytogenetics. 95 (1): 33–9. doi:10.1016/s0165-4608(97)83452-8. PMID 9140451.
Atkin NB (2000). "Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri". Cytogenetics and Cell Genetics. 91 (1–4): 44–6. doi:10.1159/000056816. PMID 11173828. S2CID 11893833.
Panani AD, Roussos C (April 2006). "Non-random structural chromosomal changes in ovarian cancer: i(5p) a novel recurrent abnormality". Cancer Letters. 235 (1): 130–5. doi:10.1016/j.canlet.2005.04.010. PMID 15927360.

harvard.edu

ui.adsabs.harvard.edu

Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S (September 2017). "Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization". Scientific Reports. 7 (1): 10395. Bibcode:2017NatSR...710395S. doi:10.1038/s41598-017-10466-z. PMC 5583289. PMID 28871159.
Olszewska M, Wanowska E, Kishore A, Huleyuk N, Georgiadis AP, Yatsenko AN, Mikula M, Zastavna D, Wiland E, Kurpisz M (November 2015). "Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient". Scientific Reports. 5: 17408. Bibcode:2015NatSR...517408O. doi:10.1038/srep17408. PMC 4663790. PMID 26616419.

medlineplus.gov

"15q11-q13 duplication syndrome: MedlinePlus Genetics".

mun-h-center.se

"Marker chromosome 15 syndrome". 5 June 2018.

nih.gov

pubmed.ncbi.nlm.nih.gov

Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T (February 2016). "Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors". Molecular Syndromology. 6 (5): 210–21. doi:10.1159/000441408. PMC 4772618. PMID 26997941.
Reddy KS, Aradhya S, Meck J, Tiller G, Abboy S, Bass H (January 2013). "A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity". Genetics in Medicine. 15 (1): 3–13. doi:10.1038/gim.2012.78. PMID 22935720.
Slimani W, Jelloul A, Al-Rikabi A, Sallem A, Hasni Y, Chachia S, Ernez A, Chaieb A, Bibi M, Liehr T, Saad A, Mougou-Zerelli S (July 2020). "Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives". Journal of Assisted Reproduction and Genetics. 37 (7): 1729–1736. doi:10.1007/s10815-020-01811-9. PMC 7376793. PMID 32399795.
Lu Y, Liang Y, Ning S, Deng G, Xie Y, Song J, Zuo N, Feng C, Qin Y (2020). "Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder". Molecular Cytogenetics. 13: 21. doi:10.1186/s13039-020-00489-z. PMC 7288499. PMID 32536972.
Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S (September 2017). "Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization". Scientific Reports. 7 (1): 10395. Bibcode:2017NatSR...710395S. doi:10.1038/s41598-017-10466-z. PMC 5583289. PMID 28871159.
Liehr T, Al-Rikabi A (2019). "Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review". Frontiers in Genetics. 10: 1131. doi:10.3389/fgene.2019.01131. PMC 6859531. PMID 31781176.
Matsubara K, Yanagida K, Nagai T, Kagami M, Fukami M (2020). "De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue". Frontiers in Genetics. 11: 132. doi:10.3389/fgene.2020.00132. PMC 7056893. PMID 32174976.
Olszewska M, Wanowska E, Kishore A, Huleyuk N, Georgiadis AP, Yatsenko AN, Mikula M, Zastavna D, Wiland E, Kurpisz M (November 2015). "Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient". Scientific Reports. 5: 17408. Bibcode:2015NatSR...517408O. doi:10.1038/srep17408. PMC 4663790. PMID 26616419.
He X, Pang Z, Zhang X, Lan T, Chen H, Chen M, Yang H, Huang J, Chen Y, Zhang Z, Jing W, Peng R, Zhang H (September 2018). "Consistent Amplification of FRS2 and MDM2 in Low-grade Osteosarcoma: A Genetic Study of 22 Cases With Clinicopathologic Analysis". The American Journal of Surgical Pathology. 42 (9): 1143–1155. doi:10.1097/PAS.0000000000001125. PMID 30001240. S2CID 51618887.
Kang JY, Kim HJ, Wojno TH, Yeung AM, Mendoza PR, Grossniklaus HE (2021). "Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma of the Orbit: Three Cases and Review of the Literature". Ophthalmic Plastic and Reconstructive Surgery. 37 (3S): S134–S140. doi:10.1097/IOP.0000000000001804. PMID 32991496. S2CID 222143763.
Huang XL, de Michelena MI, Mark H, Harston R, Benke PJ, Price SJ, Milunsky A (December 2005). "Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses". Clinical Genetics. 68 (6): 513–9. doi:10.1111/j.1399-0004.2005.00523.x. PMID 16283881. S2CID 11293671.
Chen CP, Ko TM, Chen YY, Su JW, Wang W (September 2013). "Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome". Gene. 527 (1): 384–8. doi:10.1016/j.gene.2013.05.061. PMID 23747353.
Xue H, Chen X, Lin M, Lin N, Huang H, Yu A, Xu L (December 2020). "Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis". Aging. 13 (2): 2135–2148. doi:10.18632/aging.202220. PMC 7880375. PMID 33318309.
Knijnenburg J, van Bever Y, Hulsman LO, van Kempen CA, Bolman GM, van Loon RL, Beverloo HB, van Zutven LJ (September 2012). "A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family". European Journal of Human Genetics. 20 (9): 986–9. doi:10.1038/ejhg.2012.43. PMC 3421127. PMID 22395867.
Chen CP, Lin HY, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Fran S, Chen YY, Town DD, Pan CW, Wang W (July 2020). "Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15)". Taiwanese Journal of Obstetrics & Gynecology. 59 (4): 580–585. doi:10.1016/j.tjog.2020.05.019. PMID 32653133.
Xu H, Xiao B, Ji X, Hu Q, Chen Y, Qiu W (July 2014). "Nonmosaic tetrasomy 15q25.2 → qter identified with SNP microarray in a patient with characteristic facial appearance and review of the literature". European Journal of Medical Genetics. 57 (7): 329–33. doi:10.1016/j.ejmg.2014.04.011. PMID 24793337.
George-Abraham JK, Zimmerman SL, Hinton RB, Marino BS, Witte DP, Hopkin RJ (August 2012). "Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation". American Journal of Medical Genetics. Part A. 158A (8): 1971–6. doi:10.1002/ajmg.a.35428. PMID 22711292. S2CID 22007065.
Zaki MS, Mohamed AM, Kamel AK, El-Gerzawy AM, El-Ruby MO (2012). "Emanuel syndrome due to unusual segregation of paternal origin". Genetic Counseling (Geneva, Switzerland). 23 (2): 319–28. PMID 22876593.
Luo Y, Lin J, Sun Y, Qian Y, Wang L, Chen M, Dong M, Jin F (2020). "Non-invasive prenatal screening for Emanuel syndrome". Molecular Cytogenetics. 13: 9. doi:10.1186/s13039-020-0476-7. PMC 7057502. PMID 32158503.
Vinkšel M, Volk M, Peterlin B, Lovrecic L (June 2019). "A Systematic Clinical Review of Prenatally Diagnosed Tetrasomy 9p". Balkan Journal of Medical Genetics. 22 (1): 11–20. doi:10.2478/bjmg-2019-0012. PMC 6714344. PMID 31523615.
Bellil H, Herve B, Herzog E, Ayoubi JM, Vialard F, Poulain M (March 2020). "A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report". Journal of Assisted Reproduction and Genetics. 37 (3): 573–577. doi:10.1007/s10815-020-01690-0. PMC 7125280. PMID 31981038.
Roulet-Coudrier F, Rouibi A, Thuillier C, Bourthoumieu S, Lebbar A, Dupont JM, Yardin C (February 2015). "Unusual isochromosome 5p marker chromosome". American Journal of Medical Genetics. Part A. 167A (2): 455–9. doi:10.1002/ajmg.a.36843. PMID 25424187. S2CID 33445674.
Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB (January 2020). "Diagnosis and clinical delineation of mosaic tetrasomy 5p". European Journal of Medical Genetics. 63 (1): 103634. doi:10.1016/j.ejmg.2019.02.006. PMID 30797979. S2CID 73476547.
Tesner P, Drabova J, Stolfa M, Kudr M, Kyncl M, Moslerova V, Novotna D, Kremlikova Pourova R, Kocarek E, Rasplickova T, Sedlacek Z, Vlckova M (2018). "A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature". Molecular Cytogenetics. 11: 29. doi:10.1186/s13039-018-0377-1. PMC 5941596. PMID 29760779.
Bawazeer S, Alshalan M, Alkhaldi A, AlAtwi N, AlBalwi M, Alswaid A, Alfadhel M (2018). "Tetrasomy 18p: case report and review of literature". The Application of Clinical Genetics. 11: 9–14. doi:10.2147/TACG.S153469. PMC 5811181. PMID 29467581.
Rydzanicz M, Olszewski P, Kedra D, Davies H, Filipowicz N, Bruhn-Olszewska B, Cavalli M, Szczałuba K, Młynek M, Machnicki MM, Stawiński P, Kostrzewa G, Krajewski P, Śladowski D, Chrzanowska K, Dumanski JP, Płoski R (January 2021). "Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications". Molecular Genetics & Genomic Medicine. 9 (1): e1526. doi:10.1002/mgg3.1526. PMC 7963419. PMID 33319479.
Arghir A, Popescu R, Resmerita I, Budisteanu M, Butnariu LI, Gorduza EV, Gramescu M, Panzaru MC, Papuc SM, Sireteanu A, Tutulan-Cunita A, Rusu C (May 2021). "Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review". Genes. 12 (6): 811. doi:10.3390/genes12060811. PMC 8226674. PMID 34073526.
Davies W (April 2021). "The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes" (PDF). European Journal of Medical Genetics. 64 (4): 104169. doi:10.1016/j.ejmg.2021.104169. PMID 33610733. S2CID 231987679.
Wang H, Wang T, Yang N, He Y, Chen L, Hong L, Shao X, Li H, Zhu H, Li H (June 2017). "The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype". Oncology Letters. 13 (6): 4385–4389. doi:10.3892/ol.2017.5965. PMC 5452876. PMID 28588710.
Liehr T, Weise A (May 2007). "Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics". International Journal of Molecular Medicine. 19 (5): 719–31. PMID 17390076.
Armanet N, Tosca L, Brisset S, Liehr T, Tachdjian G (2015). "Small Supernumerary Marker Chromosomes in Human Infertility". Cytogenetic and Genome Research. 146 (2): 100–8. doi:10.1159/000438718. PMID 26398339.
Sun M, Zhang H, Xi Q, Li L, Hu X, Zhang H, Liu R (October 2020). "Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems: Three case reports and literature review". Medicine. 99 (40): e22532. doi:10.1097/MD.0000000000022532. PMC 7535553. PMID 33019458.
Pei J, Flieder DB, Talarchek JN, Cooper HS, Patchefsky AS, Wei S (March 2021). "Clinical Application of Chromosome Microarray Analysis in the Diagnosis of Lipomatous Tumors". Applied Immunohistochemistry & Molecular Morphology. 29 (8): 592–598. doi:10.1097/PAI.0000000000000923. PMID 33734108. S2CID 232299293.
Usuda D, Takeshima K, Sangen R, Nakamura K, Hayashi K, Okamura H, Kawai Y, Kasamaki Y, Iinuma Y, Saito H, Kanda T, Urashima S (October 2018). "Atypical lipomatous tumor in the ligamentum teres of liver: A case report and review of the literature". World Journal of Clinical Cases. 6 (12): 548–553. doi:10.12998/wjcc.v6.i12.548. PMC 6212614. PMID 30397612.
Nishio J, Iwasaki H, Shibata T, Nabeshima K, Naito M (April 2016). "Duplication of chromosome segment 12q13–15 in a lipomatous tumor with minimal nuclear atypia: A case report". Oncology Letters. 11 (4): 2875–2878. doi:10.3892/ol.2016.4305. PMC 4812505. PMID 27073568.
Macchia G, Severgnini M, Purgato S, Tolomeo D, Casciaro H, Cifola I, L'Abbate A, Loverro A, Palumbo O, Carella M, Bianchini L, Perini G, De Bellis G, Mertens F, Rocchi M, Storlazzi CT (March 2018). "The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer". Genetics. 208 (3): 951–961. doi:10.1534/genetics.117.300552. PMC 5844343. PMID 29279323.
Bielack SS, Hecker-Nolting S, Blattmann C, Kager L (2016). "Advances in the management of osteosarcoma". F1000Research. 5: 2767. doi:10.12688/f1000research.9465.1. PMC 5130082. PMID 27990273.
Forus A, Bjerkehagen B, Sirvent N, Meza-Zepeda LA, Coindre JM, Berner JM, Myklebost O, Pedeutour F (November 2001). "A well-differentiated liposarcoma with a new type of chromosome 12-derived markers". Cancer Genetics and Cytogenetics. 131 (1): 13–8. doi:10.1016/s0165-4608(01)00516-7. PMID 11734312.
Morin JP, Saltzman AF (May 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.
Chen J, Guo M, Luo M, Deng S, Tian Q (April 2021). "Clinical characteristics and management of Turner patients with a small supernumerary marker chromosome". Gynecological Endocrinology. 37 (8): 730–734. doi:10.1080/09513590.2021.1911992. PMID 33870841. S2CID 233298107.
Barros BA, Moraes SG, Coeli FB, Assumpção JG, De Mello MP, Maciel-Guerra AT, Carvalho AB, Viguetti-Campos N, Vieira TA, Amstalden EM, Andrade JG, Esquiaveto-Aun AM, Marques-de-Faria AP, D'Souza-Li LF, Lemos-Marini SH, Guerra G (December 2011). "OCT4 immunohistochemistry may be necessary to identify the real risk of gonadal tumors in patients with Turner syndrome and Y chromosome sequences". Human Reproduction (Oxford, England). 26 (12): 3450–5. doi:10.1093/humrep/der310. PMID 21930534.
Röthlisberger B, Zerova T, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A (December 2001). "Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child". Journal of Medical Genetics. 38 (12): 885–8. doi:10.1136/jmg.38.12.885. PMC 1734780. PMID 11768396.
Fadl-Elmula I (August 2005). "Chromosomal changes in uroepithelial carcinomas". Cell & Chromosome. 4: 1. doi:10.1186/1475-9268-4-1. PMC 1199610. PMID 16083510.
Atkin NB (May 1997). "Cytogenetics of carcinoma of the cervix uteri: a review". Cancer Genetics and Cytogenetics. 95 (1): 33–9. doi:10.1016/s0165-4608(97)83452-8. PMID 9140451.
Atkin NB (2000). "Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri". Cytogenetics and Cell Genetics. 91 (1–4): 44–6. doi:10.1159/000056816. PMID 11173828. S2CID 11893833.
Panani AD, Roussos C (April 2006). "Non-random structural chromosomal changes in ovarian cancer: i(5p) a novel recurrent abnormality". Cancer Letters. 235 (1): 130–5. doi:10.1016/j.canlet.2005.04.010. PMID 15927360.

ncbi.nlm.nih.gov

Hochstenbach R, Nowakowska B, Volleth M, Ummels A, Kutkowska-Kaźmierczak A, Obersztyn E, Ziemkiewicz K, Gerloff C, Schanze D, Zenker M, Muschke P, Schanze I, Poot M, Liehr T (February 2016). "Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors". Molecular Syndromology. 6 (5): 210–21. doi:10.1159/000441408. PMC 4772618. PMID 26997941.
Slimani W, Jelloul A, Al-Rikabi A, Sallem A, Hasni Y, Chachia S, Ernez A, Chaieb A, Bibi M, Liehr T, Saad A, Mougou-Zerelli S (July 2020). "Small supernumerary marker chromosomes (sSMC) and male infertility: characterization of five new cases, review of the literature, and perspectives". Journal of Assisted Reproduction and Genetics. 37 (7): 1729–1736. doi:10.1007/s10815-020-01811-9. PMC 7376793. PMID 32399795.
Lu Y, Liang Y, Ning S, Deng G, Xie Y, Song J, Zuo N, Feng C, Qin Y (2020). "Rare partial trisomy and tetrasomy of 15q11-q13 associated with developmental delay and autism spectrum disorder". Molecular Cytogenetics. 13: 21. doi:10.1186/s13039-020-00489-z. PMC 7288499. PMID 32536972.
Jafari-Ghahfarokhi H, Moradi-Chaleshtori M, Liehr T, Hashemzadeh-Chaleshtori M, Teimori H, Ghasemi-Dehkordi P (2015). "Small supernumerary marker chromosomes and their correlation with specific syndromes". Advanced Biomedical Research. 4: 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Sun M, Zhang H, Li G, Guy CJ, Wang X, Lu X, Gong F, Lee J, Hassed S, Li S (September 2017). "Molecular characterization of 20 small supernumerary marker chromosome cases using array comparative genomic hybridization and fluorescence in situ hybridization". Scientific Reports. 7 (1): 10395. Bibcode:2017NatSR...710395S. doi:10.1038/s41598-017-10466-z. PMC 5583289. PMID 28871159.
Liehr T, Al-Rikabi A (2019). "Mosaicism: Reason for Normal Phenotypes in Carriers of Small Supernumerary Marker Chromosomes With Known Adverse Outcome. A Systematic Review". Frontiers in Genetics. 10: 1131. doi:10.3389/fgene.2019.01131. PMC 6859531. PMID 31781176.
Matsubara K, Yanagida K, Nagai T, Kagami M, Fukami M (2020). "De Novo Small Supernumerary Marker Chromosomes Arising From Partial Trisomy Rescue". Frontiers in Genetics. 11: 132. doi:10.3389/fgene.2020.00132. PMC 7056893. PMID 32174976.
Olszewska M, Wanowska E, Kishore A, Huleyuk N, Georgiadis AP, Yatsenko AN, Mikula M, Zastavna D, Wiland E, Kurpisz M (November 2015). "Genetic dosage and position effect of small supernumerary marker chromosome (sSMC) in human sperm nuclei in infertile male patient". Scientific Reports. 5: 17408. Bibcode:2015NatSR...517408O. doi:10.1038/srep17408. PMC 4663790. PMID 26616419.
Xue H, Chen X, Lin M, Lin N, Huang H, Yu A, Xu L (December 2020). "Prenatal diagnosis and molecular cytogenetic identification of small supernumerary marker chromosomes: analysis of three prenatal cases using chromosome microarray analysis". Aging. 13 (2): 2135–2148. doi:10.18632/aging.202220. PMC 7880375. PMID 33318309.
Knijnenburg J, van Bever Y, Hulsman LO, van Kempen CA, Bolman GM, van Loon RL, Beverloo HB, van Zutven LJ (September 2012). "A 600 kb triplication in the cat eye syndrome critical region causes anorectal, renal and preauricular anomalies in a three-generation family". European Journal of Human Genetics. 20 (9): 986–9. doi:10.1038/ejhg.2012.43. PMC 3421127. PMID 22395867.
Luo Y, Lin J, Sun Y, Qian Y, Wang L, Chen M, Dong M, Jin F (2020). "Non-invasive prenatal screening for Emanuel syndrome". Molecular Cytogenetics. 13: 9. doi:10.1186/s13039-020-0476-7. PMC 7057502. PMID 32158503.
Vinkšel M, Volk M, Peterlin B, Lovrecic L (June 2019). "A Systematic Clinical Review of Prenatally Diagnosed Tetrasomy 9p". Balkan Journal of Medical Genetics. 22 (1): 11–20. doi:10.2478/bjmg-2019-0012. PMC 6714344. PMID 31523615.
Bellil H, Herve B, Herzog E, Ayoubi JM, Vialard F, Poulain M (March 2020). "A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: a case report". Journal of Assisted Reproduction and Genetics. 37 (3): 573–577. doi:10.1007/s10815-020-01690-0. PMC 7125280. PMID 31981038.
Tesner P, Drabova J, Stolfa M, Kudr M, Kyncl M, Moslerova V, Novotna D, Kremlikova Pourova R, Kocarek E, Rasplickova T, Sedlacek Z, Vlckova M (2018). "A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy – case report and review of the literature". Molecular Cytogenetics. 11: 29. doi:10.1186/s13039-018-0377-1. PMC 5941596. PMID 29760779.
Bawazeer S, Alshalan M, Alkhaldi A, AlAtwi N, AlBalwi M, Alswaid A, Alfadhel M (2018). "Tetrasomy 18p: case report and review of literature". The Application of Clinical Genetics. 11: 9–14. doi:10.2147/TACG.S153469. PMC 5811181. PMID 29467581.
Rydzanicz M, Olszewski P, Kedra D, Davies H, Filipowicz N, Bruhn-Olszewska B, Cavalli M, Szczałuba K, Młynek M, Machnicki MM, Stawiński P, Kostrzewa G, Krajewski P, Śladowski D, Chrzanowska K, Dumanski JP, Płoski R (January 2021). "Variable degree of mosaicism for tetrasomy 18p in phenotypically discordant monozygotic twins-Diagnostic implications". Molecular Genetics & Genomic Medicine. 9 (1): e1526. doi:10.1002/mgg3.1526. PMC 7963419. PMID 33319479.
Arghir A, Popescu R, Resmerita I, Budisteanu M, Butnariu LI, Gorduza EV, Gramescu M, Panzaru MC, Papuc SM, Sireteanu A, Tutulan-Cunita A, Rusu C (May 2021). "Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature Review". Genes. 12 (6): 811. doi:10.3390/genes12060811. PMC 8226674. PMID 34073526.
Wang H, Wang T, Yang N, He Y, Chen L, Hong L, Shao X, Li H, Zhu H, Li H (June 2017). "The clinical analysis of small supernumerary marker chromosomes in 17 children with mos 45,X/46,X,+mar karyotype". Oncology Letters. 13 (6): 4385–4389. doi:10.3892/ol.2017.5965. PMC 5452876. PMID 28588710.
Sun M, Zhang H, Xi Q, Li L, Hu X, Zhang H, Liu R (October 2020). "Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems: Three case reports and literature review". Medicine. 99 (40): e22532. doi:10.1097/MD.0000000000022532. PMC 7535553. PMID 33019458.
Usuda D, Takeshima K, Sangen R, Nakamura K, Hayashi K, Okamura H, Kawai Y, Kasamaki Y, Iinuma Y, Saito H, Kanda T, Urashima S (October 2018). "Atypical lipomatous tumor in the ligamentum teres of liver: A case report and review of the literature". World Journal of Clinical Cases. 6 (12): 548–553. doi:10.12998/wjcc.v6.i12.548. PMC 6212614. PMID 30397612.
"MDM2 MDM2 proto-oncogene [Homo sapiens (Human)] – Gene – NCBI".
"CDK4 cyclin dependent kinase 4 [Homo sapiens (Human)] – Gene – NCBI".
Nishio J, Iwasaki H, Shibata T, Nabeshima K, Naito M (April 2016). "Duplication of chromosome segment 12q13–15 in a lipomatous tumor with minimal nuclear atypia: A case report". Oncology Letters. 11 (4): 2875–2878. doi:10.3892/ol.2016.4305. PMC 4812505. PMID 27073568.
Macchia G, Severgnini M, Purgato S, Tolomeo D, Casciaro H, Cifola I, L'Abbate A, Loverro A, Palumbo O, Carella M, Bianchini L, Perini G, De Bellis G, Mertens F, Rocchi M, Storlazzi CT (March 2018). "The Hidden Genomic and Transcriptomic Plasticity of Giant Marker Chromosomes in Cancer". Genetics. 208 (3): 951–961. doi:10.1534/genetics.117.300552. PMC 5844343. PMID 29279323.
Bielack SS, Hecker-Nolting S, Blattmann C, Kager L (2016). "Advances in the management of osteosarcoma". F1000Research. 5: 2767. doi:10.12688/f1000research.9465.1. PMC 5130082. PMID 27990273.
"YEATS4 YEATS domain containing 4 [Homo sapiens (Human)] - Gene - NCBI".
Röthlisberger B, Zerova T, Kotzot D, Buzhievskaya TI, Balmer D, Schinzel A (December 2001). "Supernumerary marker chromosome (1) of paternal origin and maternal uniparental disomy 1 in a developmentally delayed child". Journal of Medical Genetics. 38 (12): 885–8. doi:10.1136/jmg.38.12.885. PMC 1734780. PMID 11768396.
Fadl-Elmula I (August 2005). "Chromosomal changes in uroepithelial carcinomas". Cell & Chromosome. 4: 1. doi:10.1186/1475-9268-4-1. PMC 1199610. PMID 16083510.

rarediseases.info.nih.gov

"Cat eye syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program".

omim.org

orpha.net

"Orphanet: Turner syndrome".

semanticscholar.org

api.semanticscholar.org

He X, Pang Z, Zhang X, Lan T, Chen H, Chen M, Yang H, Huang J, Chen Y, Zhang Z, Jing W, Peng R, Zhang H (September 2018). "Consistent Amplification of FRS2 and MDM2 in Low-grade Osteosarcoma: A Genetic Study of 22 Cases With Clinicopathologic Analysis". The American Journal of Surgical Pathology. 42 (9): 1143–1155. doi:10.1097/PAS.0000000000001125. PMID 30001240. S2CID 51618887.
Kang JY, Kim HJ, Wojno TH, Yeung AM, Mendoza PR, Grossniklaus HE (2021). "Atypical Lipomatous Tumor/Well-Differentiated Liposarcoma of the Orbit: Three Cases and Review of the Literature". Ophthalmic Plastic and Reconstructive Surgery. 37 (3S): S134–S140. doi:10.1097/IOP.0000000000001804. PMID 32991496. S2CID 222143763.
Huang XL, de Michelena MI, Mark H, Harston R, Benke PJ, Price SJ, Milunsky A (December 2005). "Characterization of an analphoid supernumerary marker chromosome derived from 15q25-->qter using high-resolution CGH and multiplex FISH analyses". Clinical Genetics. 68 (6): 513–9. doi:10.1111/j.1399-0004.2005.00523.x. PMID 16283881. S2CID 11293671.
George-Abraham JK, Zimmerman SL, Hinton RB, Marino BS, Witte DP, Hopkin RJ (August 2012). "Tetrasomy 15q25.2→qter identified with SNP microarray in a patient with multiple anomalies including complex cardiovascular malformation". American Journal of Medical Genetics. Part A. 158A (8): 1971–6. doi:10.1002/ajmg.a.35428. PMID 22711292. S2CID 22007065.
Roulet-Coudrier F, Rouibi A, Thuillier C, Bourthoumieu S, Lebbar A, Dupont JM, Yardin C (February 2015). "Unusual isochromosome 5p marker chromosome". American Journal of Medical Genetics. Part A. 167A (2): 455–9. doi:10.1002/ajmg.a.36843. PMID 25424187. S2CID 33445674.
Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB (January 2020). "Diagnosis and clinical delineation of mosaic tetrasomy 5p". European Journal of Medical Genetics. 63 (1): 103634. doi:10.1016/j.ejmg.2019.02.006. PMID 30797979. S2CID 73476547.
Davies W (April 2021). "The contribution of Xp22.31 gene dosage to Turner and Klinefelter syndromes and sex-biased phenotypes" (PDF). European Journal of Medical Genetics. 64 (4): 104169. doi:10.1016/j.ejmg.2021.104169. PMID 33610733. S2CID 231987679.
Pei J, Flieder DB, Talarchek JN, Cooper HS, Patchefsky AS, Wei S (March 2021). "Clinical Application of Chromosome Microarray Analysis in the Diagnosis of Lipomatous Tumors". Applied Immunohistochemistry & Molecular Morphology. 29 (8): 592–598. doi:10.1097/PAI.0000000000000923. PMID 33734108. S2CID 232299293.
Morin JP, Saltzman AF (May 2021). "Gonadoblastoma in Turner Syndrome: A Surprise in a Streak". Urology. 154: 278–280. doi:10.1016/j.urology.2021.02.050. PMID 33961893. S2CID 233997606.
Chen J, Guo M, Luo M, Deng S, Tian Q (April 2021). "Clinical characteristics and management of Turner patients with a small supernumerary marker chromosome". Gynecological Endocrinology. 37 (8): 730–734. doi:10.1080/09513590.2021.1911992. PMID 33870841. S2CID 233298107.
Atkin NB (2000). "Significance of chromosome 5 and 17 changes in the development of carcinoma of the cervix uteri". Cytogenetics and Cell Genetics. 91 (1–4): 44–6. doi:10.1159/000056816. PMID 11173828. S2CID 11893833.