Lv2
140 积分 2021-10-14 加入
[Identification of pathogenic mutation in a Chinese pedigree affected with split hand/split foot malformation]
16小时前
已完结
无创产前筛查高风险胎儿的产前诊断结果分析及妊娠结局研究
2个月前
已完结
[Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome]
2个月前
已完结
Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
2个月前
已完结
一例手足裂胎儿的临床特征及病因学分
4个月前
已完结
产前诊断21四体1例
5个月前
已完结
Chromosome 2q12.3-q13 copy number variants in patients with neurodevelopmental disorders: genotype-phenotype correlation and new hotspots
6个月前
已完结
[Prenatal diagnosis analysis of three cases of Turner syndrome fetuses with complex mosaic small supernumerary marker chromosomes]
6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
6个月前
已完结
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion
7个月前
已完结
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