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Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population.
Zhang, Yan; Xie, Xiaoli; Zeng, Jixiao; Wu, Qiang; Zhang, Ruizhong; Zhu, Deli; Xia, Huimin.
Afiliação
  • Zhang Y; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Xie X; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Zeng J; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Wu Q; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Zhang R; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Zhu D; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
  • Xia H; Department of Pediatric Surgery, Guangzhou Institute of Pediatrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong, China.
J Cell Mol Med ; 22(4): 2190-2199, 2018 04.
Article em En | MEDLINE | ID: mdl-29377512

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Predisposição Genética para Doença / Neuregulina-1 / Polimorfismo de Nucleotídeo Único / Povo Asiático / Estudo de Associação Genômica Ampla / Doença de Hirschsprung Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas / Predisposição Genética para Doença / Neuregulina-1 / Polimorfismo de Nucleotídeo Único / Povo Asiático / Estudo de Associação Genômica Ampla / Doença de Hirschsprung Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article