Molecular diagnosis of phenylketonuria in 157 Chinese families and the results of prenatal diagnosis in these families

Lignende værker

• Experience of Mowat–Wilson syndrome prenatal diagnosis for a Chinese family
  af: Jiang, Qian, et al.
  Udgivet: (2016)
• Experience of Mowat–Wilson syndrome prenatal diagnosis for a Chinese family
  af: Qian Jiang, et al.
  Udgivet: (2017-01-01)
• Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report
  af: Li, Tao, et al.
  Udgivet: (2017)
• Prenatal diagnosis and genetic counseling for Waardenburg syndrome type I and II in Chinese families
  af: Wang, Li, et al.
  Udgivet: (2018)
• Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism
  af: Xu, Chenyang, et al.
  Udgivet: (2020)