Waardenburg syndrome type I in a child with deletion (2) (q35q36.2)
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference10 articles.
1. Mouse and hamster mutants as models for Waardenburg syndromes in humans.
2. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
3. Waardenburg syndrome associated with meningomyelocele
Cited by 21 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. Hearing loss in Waardenburg syndrome: a systematic review;Clinical Genetics;2015-07-17
2. EPHA4 haploinsufficiency is responsible for the short stature of a patient with 2q35-q36.2 deletion and Waardenburg syndrome;BMC Medical Genetics;2015-04-11
3. Deletion 2q36.2q36.3 with multiple renal cysts and severe mental retardation;European Journal of Medical Genetics;2008-11
4. Clinical phenotype associated with terminal 2q37 deletion;Clinical Genetics;2008-06-28
5. Ionizing radiation and genetic risks;Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis;2000-10
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