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[A case of Wiedemann-Steiner syndrome caused by a novel variation of the KMT2A gene].
Wang, J L; Huang, K; Wu, W; Zhu, M Q; Lin, H; Wu, D W; Dong, G P; Fu, J F.
Afiliação
  • Wang JL; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Huang K; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Wu W; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Zhu MQ; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Lin H; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Wu DW; Department of Genetics and Metabolism, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Dong GP; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
  • Fu JF; Department of Endorinology, the Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center, Hangzhou 310052, China.
Zhonghua Er Ke Za Zhi ; 59(6): 516-518, 2021 Jun 02.
Article em Zh | MEDLINE | ID: mdl-34102828
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Contratura / Microcefalia Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Contratura / Microcefalia Idioma: Zh Ano de publicação: 2021 Tipo de documento: Article