Lv1
18 积分 2024-12-02 加入
Towards predictive virtual embryos with genomics and AI
1个月前
已完结
Recurrent KIF2A mutations are responsible for classic lissencephaly
1个月前
已完结
Recurrent KIF2A mutations are responsible for classic lissencephaly
1个月前
已完结
AI succeeds in diagnosing rare diseases
1个月前
已完结
Prenatal diagnosis of Miller-Dieker syndrome/PAFAH1B1-related lissencephaly: Ultrasonography and genetically investigative results
1个月前
已完结
A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase gene
3个月前
已完结
Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure
3个月前
已完结
A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome
3个月前
已完结
Analysis of genetic variant in a child with autosomal recessive Alport syndrome
4个月前
已完结
Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in Holguin
8个月前
已完结
皖公网安备34019202002308
