Your browser doesn't support javascript.
loading
Case Report: Exome Sequencing Identified a Novel Compound Heterozygous Variation in PLOD2 Causing Bruck Syndrome Type 2.
Zhang, Jing; Hu, Huaying; Mu, Weihong; Yu, Mei; Chen, Wenqi; Mi, Dongqing; Yang, Kai; Guo, Qing.
Afiliação
  • Zhang J; Prenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Shijiazhuang, China.
  • Hu H; School of Medicine, Xiamen University, Xiamen, China.
  • Mu W; Jiaen Genetics Laboratory, Beijing Jiaen Hospital, Beijing, China.
  • Yu M; Prenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Shijiazhuang, China.
  • Chen W; Prenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Shijiazhuang, China.
  • Mi D; Prenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Shijiazhuang, China.
  • Yang K; Prenatal Diagnosis Center, Shijiazhuang Obstetrics and Gynecology Hospital, Shijiazhuang, China.
  • Guo Q; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University, Beijing, China.
Front Genet ; 12: 619948, 2021.
Article em En | MEDLINE | ID: mdl-33664768
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article