机译:三胞胎2P24.3-PTER和单体术的临床和分子遗传表征两种兄弟姐妹和单粒子术5p14.3-pter
Department of Genetics Institute for Developmental ResearchAichi Human Service CenterKasugai Aichi;
Division of Medical GeneticsKanagawa Children's Medical CenterYokohama Kanagawa Japan;
Department of Genetics Institute for Developmental ResearchAichi Human Service CenterKasugai Aichi;
Department of Genetics Institute for Developmental ResearchAichi Human Service CenterKasugai Aichi;
Department of Genetics Institute for Developmental ResearchAichi Human Service CenterKasugai Aichi;
Department of Pediatric NeurologyShizuoka Children's HospitalShizuoka Japan;
Department of Pediatric NeurologySeirei‐Mikatahara General HospitalHamamatsu Shizuoka Japan;
Department of Genetics Institute for Developmental ResearchAichi Human Service CenterKasugai Aichi;
intellectual disability; monosomy 5p; neural tube defects; trisomy 2p;
机译:三胞胎2P24.3-PTER和单体术的临床和分子遗传表征两种兄弟姐妹和单粒子术5p14.3-pter
机译:DE NOVO局部单项性4p(4p16.2→pter)和局部三体性8p(8p23.2→pter)的分子细胞遗传学分析
机译:从头开始的3p(3p26.3-> pter)部分三体和16q(16q23.1-> qter)的产前诊断和分子细胞遗传学特征
机译:分子IGF-1和IGF-1受体缺陷:从遗传到临床管理
机译:犬遗传模型中原发性闭角型青光眼的临床,遗传和分子方面的表征。
机译:由于家族易位t而纯 11q23.3-qter三体性或对等单胞胎的兄弟姐妹的临床和分子评估(10; 11)(q26; q23.3)
机译:从头部分单体3p(3p26.3→pter)和部分三体性16q(16q23.1→qter)的产前诊断和分子细胞遗传学表征
机译:利用分子遗传学和微流体分选对胚胎乳腺干细胞的分离,分子和功能表征的新策略