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De novo disruptive heterozygous MMP21 variants are potential predisposing genetic risk factors in Chinese Han heterotaxy children.
Qin, Xi-Ji; Xu, Meng-Meng; Ye, Jia-Jun; Niu, Yi-Wei; Wu, Yu-Rong; Xu, Rang; Li, Fen; Fu, Qi-Hua; Chen, Sun; Sun, Kun; Xu, Yue-Juan.
Afiliação
  • Qin XJ; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China.
  • Xu MM; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China.
  • Ye JJ; Department of Pediatrics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.
  • Niu YW; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China.
  • Wu YR; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China.
  • Xu R; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China.
  • Li F; Scientific Research Center, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.
  • Fu QH; Department of Pediatric Cardiology, Shanghai Children's Medical Center, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
  • Chen S; Medical Laboratory, Shanghai Children's Medical Center, Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
  • Sun K; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China. chensun@xinhuamed.com.cn.
  • Xu YJ; Department of Pediatric Cardiology, Xinhua Hospital, Affiliated to Shanghai Jiao Tong University School of Medicine, Room 505, Scientific Building, Shanghai, 200092, China. sunkun@xinhuamed.com.cn.
Hum Genomics ; 16(1): 41, 2022 09 19.
Article em En | MEDLINE | ID: mdl-36123719
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Heterotaxia Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Heterotaxia Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Animals / Child / Humans País/Região como assunto: Asia Idioma: En Ano de publicação: 2022 Tipo de documento: Article