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A New Mutation Identified by Whole Exome Sequencing in a Cornelia de Lange Syndrome Newborn.
Zhang, Hua; Yang, Li-Ming; Yuan, Lu; Tan, Xin; Zhang, Fu-Qing.
Affiliation
  • Zhang H; Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
  • Yang LM; Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
  • Yuan L; Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
  • Tan X; Department of Neonatology, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
  • Zhang FQ; Department of Eugenics and Genetics, Women and Infants Hospital of Zhengzhou, Zhengzhou, Henan 45000, China.
Chin Med J (Engl) ; 131(19): 2384-2385, 2018 10 05.
Article in En | MEDLINE | ID: mdl-30246735
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: De Lange Syndrome / Exome Sequencing / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Newborn Language: En Journal: Chin Med J (Engl) Year: 2018 Document type: Article Affiliation country:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: De Lange Syndrome / Exome Sequencing / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Newborn Language: En Journal: Chin Med J (Engl) Year: 2018 Document type: Article Affiliation country: