机译:肉碱生物合成的常见X连锁先天性错误可能是非畸形自闭症的危险因素
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Laboratory Genetic Metabolic Disease, Departments of Clinical Chemistry and Pediatrics, Academic Medical Center, University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands, Metabolism and Genetics Group, Research Institute for Medicines and Pharmaceutical Sciences (iMed.UL), Faculdade de Farmacia, Universidade de Lisboa, 1649-003 Lisbon, Portugal;
Department of Molecular Physiology and Biophysics, Center for Molecular Neuroscience, Vanderbilt University, Nashville, TN 37232;
Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095;
Centre for Applied Genomics and Program in Genetics and Genome Biology,Toronto, ON,Canada M5G 1X8;
Institut National de la Sante et de la Recherche Medicate U952, Centre National de la Recherche Scientifique Unite Mixte de Recherche 7224, and Universite Pierre et Marie Curie, University of Paris 6, Paris 94010, France;
Seaver Autism Center for Research and Treatment, Department of Psychiatry, and Friedman Brain Institute, Mount Sinai School of Medicine, New York, NY 10029;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB101SA, United Kingdom;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, Texas Children's Hospital, Houston, TX 77030, Department of Pediatrics, Washington University School of Medicine,St. Louis, MO 63110;
Texas Children's Hospital, Houston, TX 77030, Departments of Psychiatry,and Baylor College of Medicine, Houston, TX 77030;
The Offord Centre for Child Studies, McMaster Children's Hospital and Department of Psychiatry and Behavioural Neurosciences,McMaster University, Hamilton, ON, Canada L8S4L8;
Hospital for Sick Children, Toronto, ON,Canada M5G 1X8;
Disciplines of Genetics and Medicine, Memorial University of Newfoundland, St. John's, NF, Canada A1B3V6;
Greenwood Genetic Center, Greenwood, SC 29646;
Greenwood Genetic Center, Greenwood, SC 29646;
Seaver Autism Center for Research and Treatment, Department of Psychiatry, and Friedman Brain Institute, Mount Sinai School of Medicine, New York, NY 10029;
Institut National de la Sante et de la Recherche Medicate U952, Centre National de la Recherche Scientifique Unite Mixte de Recherche 7224, and Universite Pierre et Marie Curie, University of Paris 6, Paris 94010, France;
Centre for Applied Genomics and Program in Genetics and Genome Biology,Toronto, ON,Canada M5G 1X8, Hospital for Sick Children, Toronto, ON,Canada M5G 1X8;
Program on Neurogenetics, Child Study Center and Departments of Psychiatry and Genetics, Yale University School of Medicine, New Haven, CT 06520;
Department of Human Genetics, David Geffen School of Medicine, University of California, Los Angeles, CA 90095;
Department of Molecular Physiology and Biophysics, Center for Molecular Neuroscience, Vanderbilt University, Nashville, TN 37232;
Wellcome Trust Sanger Institute, Hinxton, Cambridge CB101SA, United Kingdom;
Laboratory Genetic Metabolic Disease, Departments of Clinical Chemistry and Pediatrics, Academic Medical Center, University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030;
Institute for Juvenile Research, Department of Psychiatry, University of Illinois, Chicago, IL 60608;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, Texas Children's Hospital, Houston, TX 77030, Departments of Pediatrics, Baylor College of Medicine, Houston, TX 77030;
Laboratory Genetic Metabolic Disease, Departments of Clinical Chemistry and Pediatrics, Academic Medical Center, University of Amsterdam, 1105 AZ, Amsterdam, The Netherlands;
Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, Texas Children's Hospital, Houston, TX 77030, Departments of Pediatrics, Baylor College of Medicine, Houston, TX 77030;
机译:干燥血样中酰基肉碱和游离肉碱的稳定性:对代谢性先天性错误的回顾性诊断和对肉碱转运蛋白缺乏的新生儿筛查的意义
机译:沙特阿拉伯艾哈萨市的先天缺陷和先天性代谢错误的危险因素和出生率
机译:X连锁嘌呤代谢的先天性错误的分子分析:HPRT1和PRPS1突变。
机译:(215)学习的障碍:与高功率自闭症谱系统的自杀危险因素有关的心理社会因素
机译:孤独症,与X脆弱相关的自闭症和仅X脆弱的母亲的育儿压力:对三个高风险组的儿童和母亲相关因素的检查
机译:创刊号:肉碱生物合成中常见的X连锁先天性错误可能是非畸形自闭症的危险因素
机译:肉碱生物合成的常见X连锁先天性错误可能是非畸形自闭症的危险因素