机译:PACS1中的复发性DE Novo突变导致术语颅神经嵴迁移,并定义了可识别的智力残疾综合症
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Center for Human Disease Modeling Duke University Durham NC 27710 United States;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Medical Genetics University Medical Center Utrecht 3508 AB Utrecht Netherlands;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Department of Pediatric Neurology Radboud University Nijmegen Medical Centre PO Box 9101 6500;
Center for Human Genetics Clinical Genetics University Hospitals Leuven Herestraat 49 BUS 602;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
Center for Human Disease Modeling Duke University Durham NC 27710 United States Departments of;
Center for Human Genetics Clinical Genetics University Hospitals Leuven Herestraat 49 BUS 602;
Department of Human Genetics 855 Nijmegen Centre for Molecular Life Sciences Radboud University;
机译:PACS1中从头发生的复发性突变会导致颅神经-神经migration迁移不良,并定义为可识别的智障综合征
机译:一种新的麦基义突变,影响了与普鲁斯 - Hoeijmmakers综合征的复发性PACS1 PACS1 PACS1突变相同的氨基酸
机译:一种新的麦基义突变,影响了与普鲁斯 - Hoeijmmakers综合征的复发性PACS1 PACS1 PACS1突变相同的氨基酸
机译:由于长QT综合征,kcnq1由于有缺陷的频道引起的频道扰动而导致显性造成的突变抑制
机译:在以人群为基础的早发性大肠癌患者样本中预测定量模型预测Lynch综合征(遗传性非息肉病性大肠直肠癌,DNA失配修复缺陷)的准确性
机译:PACS1中的复发性从头突变导致有缺陷的颅神经Ne迁移并定义了可识别的智障综合征
机译:PACS1中的复发性从头突变导致有缺陷的颅神经Ne迁移并定义了可识别的智障综合征