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机译:Med13L的剂量变化进一步描绘了其在先天性心脏缺陷和智力残疾中的作用
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
FRIGE's Institute of Human Genetics FRIGE House Satellite Ahmedabad India;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
Child Development Center University Children's Hospital Zurich Zurich Switzerland;
Division of Cardiology University Children's Hospital Zurich Zurich Switzerland;
Shree Krishna Hospital Karamsad India;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
Center for Medical Genetics and Molecular Medicine Haukeland University Hospital University of;
Institut de Génétique Médicale H?pital Jeanne de Flandre CHRU de Lille Lille France;
Institute of Medical Genetics University of Zurich Schorenstrasse 16 Schwerzenbach Zurich CH;
congenital heart defect; copy number changes; intellectual disability; MED13L; neurocristopathy;
机译:MED13L的剂量变化进一步描述了其在先天性心脏病和智力障碍中的作用
机译:识别智者残疾女孩中的德诺伊1季度1Q22Q23231.1患有智力障碍的女孩和包括先天性心脏缺陷的多个先天性异常
机译:Meis2的杂合态损失变异导致三合会的腭缺损,先天性心脏缺陷和智力残疾
机译:使用3D磁共振成像对先天性心脏病进行解剖学描绘
机译:具有无法解释的智力障碍或发育迟缓,先天性异常和自闭症谱系障碍的斯洛文尼亚儿童的基因组结构变异的特征。
机译:MED13L的剂量变化进一步描述了其在先天性心脏病和智力障碍中的作用
机译:MED13L的剂量变化进一步描述了其在先天性心脏病和智力障碍中的作用