Developmental delay and dysmorphic features in a girl with a de novo 5.4 Mb deletion of 13q12.11-q12.13.

Tominaga, Makiko; Saito, Toshiyuki; Masuno, Mitsuo; Umeda, You; Kurosawa, Kenji.

Afiliação

Tominaga M; Division of Medical Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
Saito T; Children's Medical Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.
Masuno M; Department of Clinical Laboratory, Kanagawa Children's Medical Center, Yokohama, Japan.
Umeda Y; Genetic Counseling Program, Graduate School of Health and Welfare, Kawasaki University of Medical Welfare, Kurashiki, Japan.
Kurosawa K; Children's Medical Center, Showa University Northern Yokohama Hospital, Yokohama, Japan.

Congenit Anom (Kyoto) ; 60(2): 73-74, 2020 Mar.

Article em En | MEDLINE | ID: mdl-31206199

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article