[Prevention and control of birth defects and rare diseases in the era of genomic medicine].

Wang, J; Xu, Y F; Fu, Q H

Wang, J; Xu, Y F; Fu, Q H.

Afiliação

Wang J; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai JiaoTong University School of Medicine, Shanghai 200127, China Shanghai Key Laboratory of Clinical Molecular Diagnostics for Pediatrics, Shanghai 200127, China.
Xu YF; Department of Medical Genetics and Molecular Diagnostic Laboratory, Shanghai Children's Medical Center, Shanghai JiaoTong University School of Medicine, Shanghai 200127, China Shanghai Key Laboratory of Clinical Molecular Diagnostics for Pediatrics, Shanghai 200127, China.
Fu QH; Shanghai Key Laboratory of Clinical Molecular Diagnostics for Pediatrics, Shanghai 200127, China Pediatric Translational Medicine Institute, Shanghai JiaoTong University School of Medicine, Shanghai 200127, China.

Zhonghua Yu Fang Yi Xue Za Zhi ; 55(9): 1023-1027, 2021 Sep 06.

Article em Zh | MEDLINE | ID: mdl-34619916

Assuntos

Genômica; Doenças Raras; Feminino; Sequenciamento de Nucleotídeos em Larga Escala; Humanos; Gravidez; Doenças Raras/genética; Doenças Raras/prevenção & controle

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Genômica / Doenças Raras Limite: Female / Humans / Pregnancy Idioma: Zh Revista: Zhonghua Yu Fang Yi Xue Za Zhi Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China País de publicação: China

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