Lv2
130 积分 2021-10-14 加入
ASTN2 in ASD and neurodevelopmental disorders
2个月前
已完结
[Genetic analysis of a child with mos 46,X,psu idic(X)(q21.3)[40]/45,X[3]]
2个月前
已完结
[Unexpected discovery of a fetus with DMD gene deletion using single nucleotide polymorphism array]
2个月前
已完结
[Identification of pathogenic mutation in a Chinese pedigree affected with split hand/split foot malformation]
3个月前
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
5个月前
已完结
[Phenotypic and genetic characteristics of a child with 7p15 deletion syndrome]
6个月前
已完结
Neurodevelopmental delay, musculoskeletal disorders and dysmorphia associated with a novel pathogenic interstitial deletion of chromosome 10q21.1q21.3
6个月前
已完结
一例手足裂胎儿的临床特征及病因学分
7个月前
已完结
产前诊断21四体1例
9个月前
已完结
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