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150 积分 2021-10-14 加入
一例手足裂胎儿的临床特征及病因学分
9天前
已完结
产前诊断21四体1例
1个月前
已完结
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots
2个月前
已完结
[Prenatal diagnosis analysis of three cases of Turner syndrome fetuses with complex mosaic small supernumerary marker chromosomes]
2个月前
已完结
多重连接依赖探针扩增在假肥大型肌营养不良症家系基因诊断中的应用
2个月前
已完结
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
3个月前
已完结
一例14q12三倍重复及 FOXG1基因相关疾病分析
3个月前
已完结
不育症伴46,X,idic(Y) (q11.21)核型一例
5个月前
已完结
无精子症伴46,X,idic(Y) (q11.22)二例
5个月前
已完结
Triplications of chromosome 1p36.3, including the genes GABRD and SKI, are associated with a developmental disorder and a facial gestalt
5个月前
已完结
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