References analysis of the Wikipedia article "Tetrasomy X" in the English version

doi.org

Linden MG, Bender BG, Robinson A (October 1995). "Sex chromosome tetrasomy and pentasomy". Pediatrics. 96 (4): 672–682. doi:10.1542/peds.96.4.672. PMID 7567329.

Nielsen J, Homma A, Christiansen F, Rasmussen K (1977). "Women with tetra-X (48,XXXX)". Hereditas. 85 (2): 151–156. doi:10.1111/j.1601-5223.1977.tb00962.x. PMID 885729.

Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A (18 June 2015). "Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48,XXXX". American Journal of Medical Genetics Part A. 167A (10): 2251–2259. doi:10.1002/ajmg.a.37198. PMID 26086740. S2CID 23652023.

Blackston RD, Chen AT (June 1972). "A case of 48,XXXX female with normal intelligence". Journal of Medical Genetics. 9 (2): 230–232. doi:10.1136/jmg.9.2.230. PMC 1469029. PMID 5046634.

Mandrioli D, Belpoggi F, Silbergeld EK, Perry MJ (12 October 2016). "Aneuploidy: a common and early evidence-based biomarker for carcinogens and reproductive toxicants". Environmental Health. 15 (97): 97. Bibcode:2016EnvHe..15...97M. doi:10.1186/s12940-016-0180-6. PMC 5059969. PMID 27729050.

Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L (11 May 2010). "A review of trisomy X (47,XXX)". Orphanet Journal of Rare Diseases. 5 (8): 8. doi:10.1186/1750-1172-5-8. PMC 2883963. PMID 20459843.

Álvarez-Vázquez P, Rivera A, Figueroa I, Páramo C, García-Mayor RV (10 July 2006). "Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy". Pituitary. 9 (2): 145–149. doi:10.1007/s11102-006-9330-0. PMID 16832583. S2CID 8358623.

Schoubben E, Decaestecker K, Quaegebeur K, Danneels L, Mortier G, Cornette L (18 May 2011). "Tetrasomy and pentasomy of the X chromosome". European Journal of Pediatrics. 170 (10): 1325–1327. doi:10.1007/s00431-011-1491-9. PMID 21590264. S2CID 21348257.

Kaur A, Pandi M, Singh JR (2009). "48,XXXX, a rare aneuploidy". Balkan Journal of Medical Genetics. 12 (1): 65–68. doi:10.2478/v10034-009-0006-8.

Visootsak J, Graham JM (24 October 2006). "Klinefelter syndrome and other sex chromosomal aneuploidies". Orphanet Journal of Rare Diseases. 1 (1): 42. doi:10.1186/1750-1172-1-42. PMC 1634840. PMID 17062147.

Tartaglia N, Howell S, Wilson R, Janusz J, Boada R, Martin S, Frazier JB, Pfeiffer M, Regan K, McSwegin S, Zeitler P (17 July 2015). "The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy". Journal of Multidisciplinary Healthcare. 8 (1): 323–334. doi:10.2147/JMDH.S80242. PMC 4514383. PMID 26229481.

Slae M, Heshin-Bekenstein M, Simckes A, Heimer G, Engelhard D, Eisenstein EM (2014). "Female polysomy-X and systemic lupus erythematosus". Seminars in Arthritis and Rheumatism. 43 (4): 508–512. doi:10.1016/j.semarthrit.2013.07.014. PMID 24012046.

DeLisi LE, Friedrich U, Wahlstrom J, Boccio-Smith A, Forsman A, Eklund K, Crow TJ (1994). "Schizophrenia and sex chromosome anomalies". Schizophrenia Bulletin. 20 (3): 495–505. doi:10.1093/schbul/20.3.495. PMID 7973466.

O'Connor MJ, Sherman J (July 1988). "Schizophrenia in a 48,XXXX child". Journal of the American Academy of Child & Adolescent Psychiatry. 27 (4): 474–478. doi:10.1097/00004583-198807000-00016. PMID 3182603.

Rooman RPA, Van Driessche K, Du Caju MVL (2002). "Growth and ovarian function in girls with 48,XXXX karyotype – patient report and review of the literature". Journal of Pediatric Endocrinology & Metabolism. 15 (7): 1051–1055. doi:10.1515/JPEM.2002.15.7.1051. PMID 12199336. S2CID 40823680.

Kara C, Üstyol A, Yılmaz A, Altundağ E, Oğur G (December 2014). "Premature ovarian failure due to tetrasomy X in an adolescent girl". European Journal of Pediatrics. 173 (12): 1627–1630. doi:10.1007/s00431-013-2209-y. PMID 24221609. S2CID 8157383.

Mikwar M, MacFarlane AJ, Marchetti F (4 July 2020). "Mechanisms of oocyte aneuploidy associated with advanced maternal age". Mutation Research/Reviews in Mutation Research. 785: 108320. doi:10.1016/j.mrrev.2020.108320. PMID 32800274.

Hassold T, Pettay D, May K, Robinson A (October 1990). "Analysis of non-disjunction in sex chromosome tetrasomy and pentasomy". Human Genetics. 85 (6): 648–850. doi:10.1007/bf00193591. PMID 1977687. S2CID 13366202.

Robinson WP, Binkert F, Schnizel AA, Basaran S, Mikelsaar R (May 1994). "Multiple origins of X chromosome tetrasomy". Journal of Medical Genetics. 31 (5): 424–425. doi:10.1136/jmg.31.5.424. PMC 1049884. PMID 8064828.

Archidiacono N, Rocchi M, Valente M, Filipi G (November 1979). "X pentasomy: a case and review". Human Genetics. 52 (1): 66–77. doi:10.1007/bf00284599. PMID 527976. S2CID 29475412.

Kuliev A, Verlinsky Y (1 October 2004). "Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis". Human Reproduction Update. 10 (5): 401–407. doi:10.1093/humupd/dmh036. PMID 15319376.

Chiang T, Schultz RM, Lampson MA (1 January 2012). "Meiotic origins of maternal age-related aneuploidy". Biology of Reproduction. 86 (1): 1–7. doi:10.1095/biolreprod.111.094367. PMC 3313661. PMID 21957193.

Bojesen A, Juul S, Gravholt GH (1 February 2003). "Prenatal and postnatal prevalence of Klinefelter syndrome: a national registry study". Journal of Clinical Endocrinology & Metabolism. 88 (2): 622–626. doi:10.1210/jc.2002-021491. PMID 12574191.

Pirollo LMA, Salehi LB, Sarta S, Cassone M, Capogna MV, Piccione E, Novelli G, Pietropolli P (29 January 2015). "A new case of prenatally diagnosed pentasomy X: review of the literature". Case Reports in Obstetrics and Gynecology. 2015: 935202. doi:10.1155/2015/935202. PMC 4325205. PMID 25699192.

Ottesen AM, Aksglaede L, Garn I, Tartaglia N, Tassone F, Gravholt CH, Bojesen A, Sørensen K, Jørgensen N, Rajpert-De Meyts E, Gerdes T, Lind AM, Kjaergaard S, Juul A (May 2010). "Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy". American Journal of Medical Genetics Part A. 152A (5): 1206–1212. doi:10.1002/ajmg.a.33334. PMC 5454803. PMID 20425825.

Rerrick EG (1970). "Mosaic XXX/XXXX sex chromosome complement case report and review of literature". Journal of Mental Deficiency Research. 14 (2): 141–148. doi:10.1111/j.1365-2788.1970.tb01108.x. PMID 5512214.

Olanders S, Wålinder J (1970). "Cutis verticis gyrata in a woman with supernumerary X chromosomes (46,XX/47,XXX/48,XXXX)". Acta Psychiatrica Scandinavica. 46 (2): 120–125. doi:10.1111/j.1600-0447.1970.tb02107.x. PMID 5478539. S2CID 36956268.

Cirillo Silengo A, Davi GF, Franceschini P (September 1979). "The 49,XXXXX syndrome". Acta Paediatrica. 68 (5): 769–771. doi:10.1111/j.1651-2227.1979.tb18456.x. S2CID 221391356.

Nakano S, Sasame A, Azukizawa S, Kigoshi T, Uchida K, Takahashi H, Morimoto S (September 1992). "Pentasomy X mosaic in two adult sisters with diabetes mellitus". Internal Medicine. 31 (9): 1102–1106. doi:10.2169/internalmedicine.31.1102. PMID 1421717.

Plaiasu V, Ochiana D, Motei G, Anca IA (October 2012). "A new case of tetrasomy X in a 8 year old girl". Acta Endocrinologica. 8 (4): 627–632. doi:10.4183/aeb.2012.627.

Singer J, Sachdeva S, Smith GF, Hsia JY (June 1972). "Triple X female and a Down's syndrome offspring". Journal of Medical Genetics. 9 (2): 238–239. doi:10.1136/jmg.9.2.238. PMC 1469037. PMID 4261628.

Berg JM, Karlinsky H, Korossy M, Pakula Z (1988). "Twenty-six years later: a woman with tetra-X chromosomes". Journal of Mental Deficiency Research. 32 (1): 67–74. doi:10.1111/j.1365-2788.1988.tb01389.x. PMID 3361607.

Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P (June 2011). "48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome". Acta Paediatrica. 100 (6): 851–860. doi:10.1111/j.1651-2227.2011.02235.x. PMC 3314712. PMID 21342258.

Turan MT, Eşel E, Dündar M, Candemir Z, Baştürk M, Sofuoğlu S, Özkul Y (1 December 2000). "Female-to-male transsexual with 47,XXX karyotype". Biological Psychiatry. 48 (1): 1116–1117. doi:10.1016/S0006-3223(00)00954-9. PMID 11094147. S2CID 16396520.

Ogata T, Matsuo M, Muroya K, Koyama Y, Fukutani K (1 February 2001). "47,XXX male: A clinical and molecular study". American Journal of Medical Genetics. 98 (4): 353–356. doi:10.1002/1096-8628(20010201)98:4<353::AID-AJMG1110>3.0.CO;2-D. PMID 11170081.

Müller U, Latt SA, Donlon T, Opitz JM (October 1987). "Y-specific DNA sequences in male patients with 46,XX and 47,XXX karyotypes". American Journal of Medical Genetics. 28 (2): 393–401. doi:10.1002/ajmg.1320280218. PMID 2827475.

Ford CE, Jones KW, Polani PE, de Almeida JCC, Briggs JH (1959). "A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome)". Lancet. 273 (7075): 711–713. doi:10.1016/S0140-6736(59)91893-8. PMID 13642858.

Jacobs PA, Strong JA (31 January 1959). "A case of human intersexuality having a possible XXY sex-determining mechanism". Nature. 183 (4657): 302–303. Bibcode:1959Natur.183..302J. doi:10.1038/183302a0. PMID 13632697. S2CID 38349997.

Jacobs PA, Baikie AG, Court Brown WM, MacGregor TN, Harnden DG (26 September 1959). "Evidence for the existence of the human 'super female'". Lancet. 274 (7100): 423–425. doi:10.1016/S0140-6736(59)90415-5. PMID 14406377.

Muldal S, Ockey CH (27 August 1960). "The 'double male': a new chromosome constitution in Klinefelter's syndrome". Lancet. 276 (7147): 492–493. doi:10.1016/S0140-6736(60)91624-X.

Sandberg AA, Koepf GF, Ishihara T, Hauschka TS (26 August 1961). "An XYY human male". Lancet. 278 (7200): 488–489. doi:10.1016/S0140-6736(61)92459-X. PMID 13746118.

Berkeley MI, Faed MJ (March 1970). "A female with the 48,XXXX karyotype". Journal of Medical Genetics. 7 (1): 83–85. doi:10.1136/jmg.7.1.83. PMC 1468910. PMID 5480970.

Ricci N, Dallapiccola B, Ventimiglia B, Tiepolo L, Fraccaro M (1968). "48, XXXX/49, XXXXX mosaic: asynchronies among the late-replicating X chromosomes". Cytogenetics. 7 (4): 249–259. doi:10.1159/000129989. PMID 5722744.

Polani PE (16 August 1969). "Abnormal sex chromosomes and mental disorders". Nature. 223 (5207): 680–686. Bibcode:1969Natur.223..680P. doi:10.1038/223680a0. PMID 4896514. S2CID 4242480.

Ricciardi G, Cammisa L, Bove R, Picchiotti G, Spaziani M, Isidori AM, et al. (2022). "Clinical, Cognitive and Neurodevelopmental Profile in Tetrasomies and Pentasomies: A Systematic Review". Children. 9 (11): 680–686. doi:10.3390/children9111719. PMC 9688827. PMID 36360447.

genome.gov

Biesecker BB. "Genetics Glossary: Karyotype". National Human Genome Research Institute. Retrieved 12 April 2021.

nih.gov

pubmed.ncbi.nlm.nih.gov

Linden MG, Bender BG, Robinson A (October 1995). "Sex chromosome tetrasomy and pentasomy". Pediatrics. 96 (4): 672–682. doi:10.1542/peds.96.4.672. PMID 7567329.

Nielsen J, Homma A, Christiansen F, Rasmussen K (1977). "Women with tetra-X (48,XXXX)". Hereditas. 85 (2): 151–156. doi:10.1111/j.1601-5223.1977.tb00962.x. PMID 885729.

Blackston RD, Chen AT (June 1972). "A case of 48,XXXX female with normal intelligence". Journal of Medical Genetics. 9 (2): 230–232. doi:10.1136/jmg.9.2.230. PMC 1469029. PMID 5046634.

Wood A, Kleis L, Toriello H, Cemeroglu AP (17 May 2011). "Mosaic pentasomy X/tetrasomy X syndrome and premature ovarian failure". Indian Pediatrics. 48 (5): 402–404. PMID 21654007.

Archidiacono N, Rocchi M, Valente M, Filipi G (November 1979). "X pentasomy: a case and review". Human Genetics. 52 (1): 66–77. doi:10.1007/bf00284599. PMID 527976. S2CID 29475412.

Telfer MA, Richardson CE, Helmken J, Smith GF (May 1970). "Divergent phenotypes among 48,XXXX and 47,XXX females". American Journal of Human Genetics. 22 (3): 326–335. PMC 1706538. PMID 4392739.

Carr DH, Barr ML, Plunkett ER (21 January 1961). "An XXXX sex chromosome complex in two mentally defective females". Canadian Medical Association Journal. 84 (3): 131–137. PMC 1939166. PMID 13690988.

Sandberg AA, Koepf GF, Ishihara T, Hauschka TS (26 August 1961). "An XYY human male". Lancet. 278 (7200): 488–489. doi:10.1016/S0140-6736(61)92459-X. PMID 13746118.

Berkeley MI, Faed MJ (March 1970). "A female with the 48,XXXX karyotype". Journal of Medical Genetics. 7 (1): 83–85. doi:10.1136/jmg.7.1.83. PMC 1468910. PMID 5480970.

Polani PE (16 August 1969). "Abnormal sex chromosomes and mental disorders". Nature. 223 (5207): 680–686. Bibcode:1969Natur.223..680P. doi:10.1038/223680a0. PMID 4896514. S2CID 4242480.

ncbi.nlm.nih.gov

rarediseases.info.nih.gov

semanticscholar.org

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Archidiacono N, Rocchi M, Valente M, Filipi G (November 1979). "X pentasomy: a case and review". Human Genetics. 52 (1): 66–77. doi:10.1007/bf00284599. PMID 527976. S2CID 29475412.

Cirillo Silengo A, Davi GF, Franceschini P (September 1979). "The 49,XXXXX syndrome". Acta Paediatrica. 68 (5): 769–771. doi:10.1111/j.1651-2227.1979.tb18456.x. S2CID 221391356.

Polani PE (16 August 1969). "Abnormal sex chromosomes and mental disorders". Nature. 223 (5207): 680–686. Bibcode:1969Natur.223..680P. doi:10.1038/223680a0. PMID 4896514. S2CID 4242480.

web.archive.org

US Dept. of Health and Human Services, et al. (August 2016). "Anthropometric reference data for children and adults: United States, 2011–2014" (PDF). National Health Statistics Reports. 11. Archived (PDF) from the original on 2 February 2017. Retrieved 23 March 2021.

"Australian health survey: first results". Australian Bureau of Statistics. 29 October 2012. Archived from the original on 20 January 2017. Retrieved 23 March 2021.

Rooman R, Hultén M (2005). "Tetrasomy X" (PDF). Unique. Archived (PDF) from the original on 18 March 2021.

O'Connor C (2008). "Chromosomal abnormalities: aneuploidies". Nature Education. 1 (1): 172. Archived from the original on 3 November 2020.

"Tetrasomy/Pentasomy X Support Group". National Organization for Rare Disorders. Archived from the original on 24 April 2016. Retrieved 10 April 2021.

Auchmutey P (2018). "Extraordinary care". Emory Health Digest. Archived from the original on 6 August 2020. Retrieved 26 March 2021.

Tetrasomy X (English Wikipedia)

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pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

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rarechromo.org

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semanticscholar.org

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