机译:SHANK3和IGF1恢复22q13缺失综合征患者神经元的突触缺乏
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Obstetrics and Gynecology, Stanford University, Stanford, California 94305, USA,Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, California 94305, USA;
Department of Neurobiology, Stanford University, Stanford, California 94305, USA;
Department of Pediatrics, Stanford University, Stanford, California 94305, USA,Department of Psychiatry and Behavioral Science, Stanford University, Stanford, California 94305, USA;
Department of Pediatrics, Stanford University, Stanford, California 94305, USA;
Department of Psychiatry and Behavioral Science, Stanford University, Stanford, California 94305, USA;
Novartis Institutes for Biomedical Research, Cambridge, Massachusetts 02139, USA;
机译:不涉及SHANK3基因的间质22q13缺失:一种新的连续基因综合征
机译:前瞻性调查22q13缺失综合征和SHANK3缺乏症的自闭症和基因型-表型的相关性
机译:22q13缺失综合征的分子特征支持SHANK3 / PROSAP2的单倍不足在主要神经系统症状中的作用。
机译:KCNQ1的新型缺失突变导致近乎溺水的患者家庭中的长QT综合征
机译:遗传学的新面貌:医学界对提高患者满意度的教育。 22q11.2删除综合征和特纳综合征的比较。
机译:Shank3和IGF1恢复22q13缺失综合征患者神经元的突触缺乏。
机译:对phelan K.等人的回应:致Disciglio等编辑的信:不涉及sHaNK3基因的间质22q13缺失:一种新的连续基因综合征