Lv2
130 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
1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
2个月前
已完结
Rhythmic cortical myoclonus in patients with 6Q22.1 deletion
2个月前
已完结
Clinical implications of expanded carrier screening for pregnancy-related care and individual health
3个月前
已完结
Expanded carrier screening for 224 monogenic disease genes in 1,499 Chinese couples: a single-center study
3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
5个月前
已完结
Oculoauriculovertebral spectrum with 5p15.33-pter deletion
7个月前
已完结
A case of polimalformed fetus with a microdeletion of CTNNA3 gene
8个月前
已完结
Small supernumerary marker chromosomes-progress towards a genotype-phenotype correlation
9个月前
已完结
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