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Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China.
Wang, Huijun; Lu, Yulan; Dong, Xinran; Lu, Guoping; Cheng, Guoqiang; Qian, Yanyan; Ni, Qi; Zhang, Ping; Yang, Lin; Wu, Bingbing; Zhou, Wenhao.
Afiliación
  • Wang H; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Lu Y; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Dong X; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Lu G; Pediatric Intensive Care Unit, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Cheng G; Department of Neonates, Key Laboratory of Neonatal Diseases, Ministry of Health, Children's Hospital of Fudan University, Shanghai, 201102, China.
  • Qian Y; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Ni Q; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Zhang P; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Yang L; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China.
  • Wu B; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China. 081107271@fudan.edu.cn.
  • Zhou W; Center for Molecular Medicine, Shanghai Key Laboratory of Birth Defects, Children's Hospital of Fudan University, 399 Wanyuan Road, Shanghai, 201102, China. zhouwenhao@fudan.edu.cn.
Hum Genet ; 139(4): 473-482, 2020 Apr.
Article en En | MEDLINE | ID: mdl-31965297
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pruebas Genéticas / Variaciones en el Número de Copia de ADN / Secuenciación Completa del Genoma Tipo de estudio: Clinical_trials / Guideline Límite: Female / Humans / Infant / Male / Newborn País/Región como asunto: Asia Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pruebas Genéticas / Variaciones en el Número de Copia de ADN / Secuenciación Completa del Genoma Tipo de estudio: Clinical_trials / Guideline Límite: Female / Humans / Infant / Male / Newborn País/Región como asunto: Asia Idioma: En Revista: Hum Genet Año: 2020 Tipo del documento: Article País de afiliación: China