Your browser doesn't support javascript.
loading
[Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ].
Hu, Hao; Wang, Hua; Jia, Zhengjun; Xie, Qiong.
Affiliation
  • Hu H; Medical Genetic Laboratory, Maternal and Children Health Hospital of Hunan, Changsha, Hunan 410008, P. R. China. wanghua213@aliyun.com.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi ; 31(4): 424-7, 2014 Aug.
Article in Zh | MEDLINE | ID: mdl-25119903
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Transport Proteins / Albinism, Oculocutaneous / Asian People / Fetal Diseases Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Pregnancy Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: China
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Transport Proteins / Albinism, Oculocutaneous / Asian People / Fetal Diseases Type of study: Diagnostic_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged / Pregnancy Language: Zh Journal: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Journal subject: GENETICA MEDICA Year: 2014 Document type: Article Country of publication: China