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[Prenatal gene diagnosis of 200 fetuses at high risk of osteogenesis imperfect].
Zhao, X L; Gao, J S; Li, L L; Li, S; Wang, H; Xiao, J F; Zhang, J; Mi, H; Yang, Y J; Zhao, F Y; Guan, X; Cao, Y X; Wu, Y Y; Lu, C X; Yang, T; Zhang, X.
Afiliación
  • Zhao XL; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Gao JS; Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Beijing 100730, China.
  • Li LL; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Li S; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Wang H; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Xiao JF; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Zhang J; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Mi H; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Yang YJ; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Zhao FY; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Guan X; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Cao YX; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Wu YY; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Lu CX; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Yang T; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
  • Zhang X; Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences -School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
Zhonghua Yi Xue Za Zhi ; 99(42): 3328-3334, 2019 Nov 12.
Article en Zh | MEDLINE | ID: mdl-31715670

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Año: 2019 Tipo del documento: Article País de afiliación: China