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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.
Afiliación
  • 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 en Zh | MEDLINE | ID: mdl-34102828
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Contractura / Microcefalia Límite: Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: China
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Anomalías Múltiples / Contractura / Microcefalia Límite: Humans Idioma: Zh Revista: Zhonghua Er Ke Za Zhi Año: 2021 Tipo del documento: Article País de afiliación: China Pais de publicación: China