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Rare Variants and Polymorphisms of FBN1 Gene May Increase the Risk of Non-Syndromic Aortic Dissection.
Pan, Meichen; Li, Lianjie; Li, Zehao; Chen, Shu; Li, Zongzhe; Wang, Yuning; He, Henghui; Lin, Lihua; Wang, Haihao; Liu, Qian.
Afiliação
  • Pan M; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Li L; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Li Z; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Chen S; Division of Thoracic Surgery, Union Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Li Z; Division of Cardiology, Departments of Internal Medicine and Genetic Diagnosis Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
  • Wang Y; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • He H; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Lin L; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Wang H; Division of Thoracic Surgery, Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
  • Liu Q; Department of Forensic Medicine, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, China.
Front Genet ; 13: 778806, 2022.
Article em En | MEDLINE | ID: mdl-35154271
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 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: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Front Genet Ano de publicação: 2022 Tipo de documento: Article