Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito
Author:
Affiliation:
1. Universidade de Campinas, Brazil
Publisher
FapUNIFESP (SciELO)
Subject
Genetics,Molecular Biology
Link
http://www.scielo.br/pdf/gmb/v39n1/1415-4757-gmb-39-1-35.pdf
Reference7 articles.
1. New association between ring chromosome 20 syndrome and hypomelanosis of Ito;Cappanera S;Pediatr Neurol,2011
2. A large analphoid inv dup(3)(q22.3qter) marker chromosome characterized by array-CGH in a child with malformations, mental retardation, ambiguous genitalia and Blaschko's lines;Gimelli G;Eur J Med Genet,2007
3. Analphoid supernumerary marker chromosome characterized by aCGH and FISH as inv dup(3)(q25.33qter) de novo in a child with dysmorphic features and streaky pigmentation: case report;Murthy SK;Mol Cytogenet,2008
4. Hypomelanosis of Ito: neurological complications in 34 cases;Pascual-Castroviejo I;Can J Neurol Sci,1988
5. Skin pigmentary anomalies and mosaicism for an acentric marker chromosome originating from 3q;Portnoi MF;J Med Genet,1999
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism;Frontiers in Genetics;2024-04-16
2. Genome characterization and CRISPR-Cas9 editing of a human neocentromere;Chromosoma;2022-08-17
3. Fundus Pigmentary Whorls in a Patient With Mosaicism for Tetrasomy 3q;JAMA Ophthalmology;2021-08-01
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