Lv21
140 积分 2025-04-24 加入
8.6Mb interstitial deletion of chromosome 4q13.3q21.23 in a boy with cognitive impairment, short stature, hearing loss, skeletal abnormalities and facial dysmorphism
3个月前
已完结
Y染色体长臂嵌合缺失胎儿1例的遗传学分析
4个月前
已完结
Rhythmic cortical myoclonus in patients with 6Q22.1 deletion
4个月前
已完结
Clinical implications of expanded carrier screening for pregnancy-related care and individual health
4个月前
已完结
Expanded carrier screening for 224 monogenic disease genes in 1,499 Chinese couples: a single-center study
4个月前
已完结
一例der(X) t(X；Y)(p22.3；q11.2)胎儿的产前诊断及遗传学分析
7个月前
已完结
Oculoauriculovertebral spectrum with 5p15.33-pter deletion
9个月前
已完结
A case of polimalformed fetus with a microdeletion of CTNNA3 gene
10个月前
已完结
Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation
11个月前
已完结
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