Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders.

Zhang, Yuanyuan; Liu, Xiaoliang; Gao, Haiming; Cui, Wanting; Zhang, Bijun; Zhao, Yanyan

Zhang, Yuanyuan; Liu, Xiaoliang; Gao, Haiming; Cui, Wanting; Zhang, Bijun; Zhao, Yanyan.

Afiliação

Zhang Y; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Liu X; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Gao H; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Cui W; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Zhang B; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China.
Zhao Y; Department of Clinical Genetics, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, China. yyzhao@sj-hospital.org.

Mol Cytogenet ; 14(1): 57, 2021 Dec 18.

Article em En | MEDLINE | ID: mdl-34922566

Palavras-chave

15q24 microdeletion; Developmental delay; MLPA

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Mol Cytogenet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

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