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Association of maternal methionine synthase reductase gene polymorphisms with the risk of congenital heart disease in offspring: a hospital-based case-control study.
Wei, Jianhui; Wang, Tingting; Song, Xinli; Liu, Yiping; Shu, Jing; Sun, Mengting; Diao, Jingyi; Li, Jingqi; Li, Yihuan; Chen, Letao; Zhang, Senmao; Huang, Peng; Qin, Jiabi.
Afiliación
  • Wei J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Wang T; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Song X; Hunan Provincial Maternal and Child Health Care Hospital, Changsha, China.
  • Liu Y; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Shu J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Sun M; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Diao J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Li J; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Li Y; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Chen L; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Zhang S; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Huang P; Department of Epidemiology and Health Statistics, Xiangya School of Public Health, Central South University, Changsha, China.
  • Qin J; Hunan Children's Hospital, Changsha, China.
J Matern Fetal Neonatal Med ; 36(1): 2211201, 2023 Dec.
Article en En | MEDLINE | ID: mdl-37183022
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 2_ODS3 Problema de salud: 1_doencas_nao_transmissiveis / 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Polimorfismo de Nucleótido Simple / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Matern Fetal Neonatal Med Asunto de la revista: OBSTETRICIA / PERINATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 1_ASSA2030 / 2_ODS3 Problema de salud: 1_doencas_nao_transmissiveis / 2_muertes_prematuras_enfermedades_notrasmisibles Asunto principal: Polimorfismo de Nucleótido Simple / Cardiopatías Congénitas Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Female / Humans Idioma: En Revista: J Matern Fetal Neonatal Med Asunto de la revista: OBSTETRICIA / PERINATOLOGIA Año: 2023 Tipo del documento: Article País de afiliación: China