机译:基于人口和家庭的研究将MTHFR基因与单纯形家庭的特发性自闭症相关联
Department of Psychiatry &amp Physiology, Queen’s University, Autism Research Program, Ongwanada Resource Centre, 191 Portsmouth Avenue, Kingston, ON, K7M 8A6, Canada;
Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada;
Department of Psychology, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA;
Department of Psychology, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA;
Department of Human Genetics, New York State Institute for Basic Research in Developmental Disabilities, Staten Island, NY, USA;
Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada;
Department of Psychiatry &amp Physiology, Queen’s University, Autism Research Program, Ongwanada Resource Centre, 191 Portsmouth Avenue, Kingston, ON, K7M 8A6, Canada;
Autism spectrum disorders (ASDs); Gene association; Methylenetetrahydrofolate reductase (MTHFR); Functional polymorphism; Epigenetics; Methylation;
机译:基于人群和家庭的研究将MTHFR基因与单纯型家庭的特发性自闭症联系起来
机译:日本牙齿发育不全的遗传流行病学:基于人群和家庭的研究
机译:基于家族的研究中外显子拷贝数变异的全基因组分析指向新型自闭症易感基因
机译:在基于家庭的研究中使用Markov-Blanket检测高维遗传关联
机译:出生缺陷中MTHFR的研究:丙戊酸和MTHFR启动子分析的药物遗传学研究。
机译:基于家族的研究中外显子拷贝数变异的全基因组分析指向新型自闭症易感基因
机译:基于家庭的研究中外显子拷贝数变异的全基因组分析指出了新型自闭症易感基因
机译:mTHFR功能多态性C677T与单纯性家系特发性孤独症病因学中的基因组不稳定性。