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Clinical and Genetic Etiologies of Neonatal Unconjugated Hyperbilirubinemia in the China Neonatal Genomes Project.
Mei, Hongfang; Dong, Xinran; Wu, Bingbing; Wang, Huijun; Lu, Yulan; Hu, Liyuan; Wang, Jin; Cao, Yun; Zhang, Rong; Cheng, Guoqiang; Wang, Laishuan; Li, Zhihua; Yang, Lin; Zhou, Wenhao.
Afiliação
  • Mei H; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Dong X; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Wu B; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Wang H; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Lu Y; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Hu L; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Wang J; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Cao Y; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Zhang R; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Cheng G; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Wang L; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Li Z; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Yang L; Clinical Genetic Center, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China.
  • Zhou W; Department of Neonatology, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China; Key Laboratory of Birth Defects, Children's Hospital of Fudan University, National Children's Medical Center, Shanghai, China; Clinical Genetic Center, Children's Hospital of Fuda
J Pediatr ; 243: 53-60.e9, 2022 04.
Article em En | MEDLINE | ID: mdl-34953813

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glucuronosiltransferase / Hiperbilirrubinemia Neonatal / Glucosefosfato Desidrogenase Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies Limite: Humans / Newborn País/Região como assunto: Asia Idioma: En Revista: J Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glucuronosiltransferase / Hiperbilirrubinemia Neonatal / Glucosefosfato Desidrogenase Tipo de estudo: Etiology_studies / Guideline / Prognostic_studies Limite: Humans / Newborn País/Região como assunto: Asia Idioma: En Revista: J Pediatr Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos