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Use of medical exome sequencing for identification of underlying genetic defects in NICU: Experience in a cohort of 2303 neonates in China.
Yang, Lin; Wei, Zejun; Chen, Xiang; Hu, Liyuan; Peng, Xiaomin; Wang, Jin; Lu, Chunmei; Kong, Yanting; Dong, Xinran; Ni, Qi; Lu, Yulan; Wu, Bingbing; Wang, Huijun; Meirelles, Katia; Tian, Xia; Zhang, Jing; Chang, Fengqi; Liu, Liu; Li, Changhua; You, Wesley; Cheng, Guoqiang; Wang, Laishuan; Cao, Yun; Chen, Chao; Fang, Ping; Tang, Sha; Zhou, Wenhao.
Afiliación
  • Yang L; Clinical Genetic Center, Children's Hospital of Fudan University, Shanghai, China.
  • Wei Z; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Chen X; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Hu L; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Peng X; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Wang J; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Lu C; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Kong Y; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Dong X; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Ni Q; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Lu Y; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Wu B; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Wang H; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Meirelles K; Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, Shanghai, China.
  • Tian X; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, Shanghai, China.
  • Zhang J; Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, Shanghai, China.
  • Chang F; Premier Research, Morrisville, North Carolina, USA.
  • Liu L; Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, USA.
  • Li C; KingMed Diagnostics, Guangzhou, China.
  • You W; KingMed Diagnostics, Guangzhou, China.
  • Cheng G; Sema4, Branford, Connecticut, USA.
  • Wang L; KingMed Diagnostics, Guangzhou, China.
  • Cao Y; Google LLC, Mountain View, California, USA.
  • Chen C; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Fang P; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Tang S; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
  • Zhou W; Division of Neonatology, Children's Hospital of Fudan University, Shanghai, China.
Clin Genet ; 101(1): 101-109, 2022 01.
Article en En | MEDLINE | ID: mdl-34671977
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Unidades de Cuidado Intensivo Neonatal / Predisposición Genética a la Enfermedad / Estudios de Asociación Genética / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Unidades de Cuidado Intensivo Neonatal / Predisposición Genética a la Enfermedad / Estudios de Asociación Genética / Secuenciación del Exoma / Enfermedades Genéticas Congénitas Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article País de afiliación: China