A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay-Reference-Cited by-同舟云学术

A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay

Published:2008-07 Issue:4 Volume:51 Page:368-372
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Chen Chih-Ping,Lin Shuan-Pei,Tsai Fuu-Jen,Chern Schu-Rern,Lee Chen-Chi,Wang Wayseen

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference12 articles.

1. Clinical features in a de novo interstitial deletion 15q13 to q15;Autio;Clin. Genet.,1988

2. No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q;Durner;Am. J. Med. Genet.,2000

3. Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q;Elmslie;Hum. Mol. Genet.,1997

4. Characterization of a 5.3Mb deletion in 15q14 by comparative genomic hybridization using a whole genome “tiling path” BAC array in a girl with heart defect, cleft palate, and developmental delay;Erdogan;Am. J. Med. Genet.,2007

5. Interstitial 15q deletion without a classic Prader–Willi phenotype;Galán;Am. J. Med. Genet.,1991

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