Cat eye syndrome (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Cat eye syndrome" in English language version.

refsWebsite

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11nih.gov

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5doi.org

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1orpha.net

3,537^th place

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1c22c.org

low place

1semanticscholar.org

11^th place

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c22c.org

"Disorders of chromosome 22: Cat Eye Syndrome/Schmid Fraccaro Syndrome". www.c22c.org. Chromosome 22 Central. 18 July 2017. Retrieved 22 December 2017.

doi.org

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 (1): 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
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.
Schachenmann G.; Schmid W.; Fraccaro M.; et al. (1965). "Chromosomes in Coloboma and Anal Atresia". Lancet. 2 (7406): 290. doi:10.1016/S0140-6736(65)92415-3. PMID 14330081.
Bühler EM, Méhes K, Müller H, Stalder GR (1972). "Cat-eye syndrome, a partial trisomy 22". Humangenetik. 15 (2): 150–62. doi:10.1007/BF00295742. PMID 5049068. S2CID 35284790.

nih.gov

pubmed.ncbi.nlm.nih.gov

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 (1): 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
Rosias PR, Sijstermans JM, Theunissen PM, et al. (2001). "Phenotypic variability of the cat eye syndrome. Case report and review of the literature". Genet. Couns. 12 (3): 273–82. PMID 11693792.
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.
Schachenmann G.; Schmid W.; Fraccaro M.; et al. (1965). "Chromosomes in Coloboma and Anal Atresia". Lancet. 2 (7406): 290. doi:10.1016/S0140-6736(65)92415-3. PMID 14330081.
Bühler EM, Méhes K, Müller H, Stalder GR (1972). "Cat-eye syndrome, a partial trisomy 22". Humangenetik. 15 (2): 150–62. doi:10.1007/BF00295742. PMID 5049068. S2CID 35284790.

ncbi.nlm.nih.gov

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 (1): 140. doi:10.4103/2277-9175.161542. PMC 4544121. PMID 26322288.
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.

rarediseases.info.nih.gov

"Cat eye syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program".
"Cat eye syndrome | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 17 April 2018.

orpha.net

"Cat eye syndrome". Orphanet. Retrieved 20 March 2019.

semanticscholar.org

api.semanticscholar.org

Bühler EM, Méhes K, Müller H, Stalder GR (1972). "Cat-eye syndrome, a partial trisomy 22". Humangenetik. 15 (2): 150–62. doi:10.1007/BF00295742. PMID 5049068. S2CID 35284790.