Additional individuals with CHD7 variants in Chinese and other southeast Asian patients.

Wei, Heming; Tan, Ee-Shien; Jamuar, Saumya; Lai, Angeline H M; Ng, Ivy; Tan, Ene-Choo

Wei, Heming; Tan, Ee-Shien; Jamuar, Saumya; Lai, Angeline H M; Ng, Ivy; Tan, Ene-Choo.

Afiliación

Wei H; Research Laboratory, KK Women's and Children's Hospital, Singapore, Singapore.
Tan ES; Genetics Service, KK Women's and Children's Hospital, Singapore, Singapore.
Jamuar S; Pediatrics Academic Clinical Programme, SingHealth Duke-NUS Graduate Medical School, Singapore, Singapore.
Lai AHM; Genetics Service, KK Women's and Children's Hospital, Singapore, Singapore.
Ng I; Pediatrics Academic Clinical Programme, SingHealth Duke-NUS Graduate Medical School, Singapore, Singapore.
Tan EC; Genetics Service, KK Women's and Children's Hospital, Singapore, Singapore.

Am J Med Genet A ; 182(10): 2461-2465, 2020 10.

Article en En | MEDLINE | ID: mdl-32804436

Asunto(s)

Síndrome CHARGE; Pueblo Asiatico/genética; China/epidemiología; ADN Helicasas; Proteínas de Unión al ADN/genética; Humanos

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndrome CHARGE Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article País de afiliación: Singapur

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