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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