机译:血缘家庭的纯合子作图揭示了非综合征常染色体隐性遗传性智力低下的极端异质性,并确定了8个新基因位点
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetic and Pathology Laboratory Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Genetics Research Centre University of Social Welfare and Rehabilitation Sciences Tehran Iran;
Department of Paediatric Endocrinology Otto Heubner Centre for Paediatrics Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Gene Mapping Centre Max Delbrück Centre for Molecular Medicine Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
Department Human Molecular Genetics Max Planck Institute for Molecular Genetics Ihnestr. 73 14195 Berlin Germany;
机译:在近亲家庭中的纯合子作图揭示了非综合征常染色体隐性智力低下的极端异质性,并鉴定了8个新基因位点。
机译:巴基斯坦近亲家庭中非综合征性常染色体隐性遗传性智力低下(NS-ARMR)的三个新基因座的定位。
机译:巴基斯坦近亲家庭中非综合征性常染色体隐性遗传性智力低下(NS-ARMR)的三个新基因座的定位
机译:TRNA的自上而下的质谱显示样品异质性并识别/定位后术后修改
机译:在实验生物中识别人类疾病基因和定量性状基因座定位的研究设计。
机译:染色体区域19p13.12-p13.2中常染色体隐性非综合征性智力低下的新基因座的定位:进一步的遗传异质性
机译:在非综合征性智障的叙利亚近亲家庭中的64个纯合子作图显示11个新基因座和高度异质性