CNOT2 CNOT2 haploinsufficiency causes a neurodevelopmental disorder with characteristic facial features

著录项

• 来源
  《American journal of medical genetics, Part A》 |2019年第11期|共4页
• 作者

  Uehara Tomoko; Tsuchihashi Takatoshi; Yamada Mamiko; Suzuki Hisato; Takenouchi Toshiki; Kosaki Kenjiro;

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• 作者单位

  Center for Medical GeneticsKeio University School of MedicineTokyo Japan;

  Department of PediatricsKawasaki Municipal HospitalKanagawa Japan;

  Center for Medical GeneticsKeio University School of MedicineTokyo Japan;

  Center for Medical GeneticsKeio University School of MedicineTokyo Japan;

  Department of PediatricsKeio University HospitalTokyo Japan;

  Center for Medical GeneticsKeio University School of MedicineTokyo Japan;

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• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 医学遗传学;
• 关键词