Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome
Author:
Affiliation:
1. Department of Primary Child Health Care; Children's Hospital of Chongqing Medical University; Chongqing; China
2. Center for Clinical Molecular Medicine; Children's Hospital of Chongqing Medical University; Chongqing; China
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2012.03684.x/fullpdf
Reference9 articles.
1. Clinical utility gene card for: Wolf-Hirschhorn (4p-) syndrome;Battaglia;Eur. J. Hum. Genet.,2011
2. Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH);Maas;J. Med. Genet.,2008
3. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: Experience with 87 patients and recommendations for routine health supervision;Battaglia;Am. J. Med. Genet. C Semin. Med. Genet.,2008
4. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syn-drome;Zollino;Am. J. Med. Genet.,2000
5. The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndrome;Zollino;J. Med. Genet.,2008
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1. Familial Translocation t(2;4) (q37.3;p16.3), Resulting in a Partial Trisomy of 2q (or 4p) and a Partial Monosomy of 4p (or 2q), Causes Dysplasia;Frontiers in Genetics;2021-11-23
2. 18q22.1-qter deletion and 4p16.3 microduplication in a boy with speech delay and mental retardation: case report and review of the literature;Molecular Cytogenetics;2018-10-19
3. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions;American Journal of Medical Genetics Part A;2016-06-10
4. Wolf-Hirschhorn Syndrome with Epibulbar Dermoid: An Unusual Association in a Patient with 4p Deletion and Functional Xp Disomy;Cytogenetic and Genome Research;2016
5. Meiotic and pedigree segregation analyses in carriers of t(4;8)(p16;p23.1) differing in localization of breakpoint positions at 4p subband 4p16.3 and 4p16.1;Journal of Assisted Reproduction and Genetics;2015-12-04
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