Your browser doesn't support javascript.
loading
Investigation of an inherited PCGF2: p.Pro65Leu mutation causing Turnpenny-Fry syndrome.
Qi, Ke-Yan; Shen, Ming; Yang, Kai; Yan, You-Sheng; Wu, Jue; Wang, Yi-Peng; Yin, Cheng-Hong.
Affiliation
  • Qi KY; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing 100026, China.
  • Shen M; Research Center for Translational Medicine Laboratory, Medical Innovation Research Division of Chinese PLA General Hospital Beijing 100000, China.
  • Yang K; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing 100026, China.
  • Yan YS; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing 100026, China.
  • Wu J; Research Center for Translational Medicine Laboratory, Medical Innovation Research Division of Chinese PLA General Hospital Beijing 100000, China.
  • Wang YP; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing 100026, China.
  • Yin CH; Prenatal Diagnosis Center, Beijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing 100026, China.
Am J Transl Res ; 14(8): 5591-5597, 2022.
Article in En | MEDLINE | ID: mdl-36105049
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Transl Res Year: 2022 Document type: Article Affiliation country: China Country of publication: Estados Unidos
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Am J Transl Res Year: 2022 Document type: Article Affiliation country: China Country of publication: Estados Unidos