机译:XQ26.1-26.3复制包括较短地形和双出口右心室的男孩中识别的MOSPD1和GPC3
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
Department of PediatricsJichi Medical UniversityTochigi Japan;
congenital heart disease (CHD); double outlet right ventricle (DORV); GPC3; MOSPD1; short stature; Xq26.1‐26.3 duplication;
机译:XQ26.1-26.3复制包括较短地形和双出口右心室的男孩中识别的MOSPD1和GPC3
机译:与46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3)相关的男性胎儿中Xp22.32→pter缺失和Xq26.3→qter复制的分子细胞遗传学表征心脏,身材矮小和母亲X染色体周围性倒置
机译:由于双入口左心室和复杂的双出口右心室受“ VSD”限制而导致出口阻塞的较老的单功能心室的管理
机译:双栅极MOSFET中漏极电流的紧凑模型,包括载流子量化和短沟道效应
机译:一名身材严重矮小,性腺功能低下,全球发育迟缓和智力残疾的男孩,罕见的从头重复15q15.3q21.2
机译:分子细胞遗传学表征Xp22.32→pter缺失和Xq26.3→qter重复在男性胎儿相关的46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3),左侧发育不全心脏,身材矮小,母体X染色体周围反转