A clinical and genetic study of 16 Japanese families with Waardenburg syndrome-Reference-Cited by-同舟云学术

A clinical and genetic study of 16 Japanese families with Waardenburg syndrome

Published:2019-07 Issue: Volume:704 Page:86-90
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Minami Shujiro B.,Nara Kiyomitsu,Mutai Hideki,Morimoto Noriko,Sakamoto Hirokazu,Takiguchi Tetsuya,Kaga Kimitaka^ORCID,Matsunaga Tatsuo^ORCID

Funder

National Hospital Organization of Japan

Japan Agency for Medical Research and Development

JSPS

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference28 articles.

1. Apparent non-penetrance for dystopia in Waardenburg syndrome type I, with some hints on the diagnosis of dystopia canthorum;Arias;J. Genet. Hum.,1978

2. Mutations in PAX3 associated with Waardenburg syndrome type I;Baldwin;Hum. Mutat.,1994

3. Identification and functional analysis of SOX10 missense mutations in different subtypes of Waardenburg syndrome;Chaoui;Hum. Mutat.,2011

4. Some statistical problems posed by Waardenburg's data on dystopia canthorum and associated anomalies;Cotterman;Am. J. Hum. Genet.,1951

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