Lv552
928 积分 2024-08-22 加入
Global retardation and hereditary spherocytosis associated with a novel deletion of chromosome 8p11.21 encompassing KAT6A and ANK1
3个月前
已完结
Speech and language development and genotype–phenotype correlation in 49 individuals with KAT6A syndrome
3个月前
已完结
[Analysis of a child with mental retardation due to a de novo variant of the KAT6A gene]
3个月前
已完结
Broadening the ocular phenotypic spectrum of ultra-rare BRPF1 variants: report of two cases
3个月前
已完结
Novel de novo mutation in KAT6A gene in a child with severe aplastic anemia
3个月前
已完结
Novel de novo mutation in KAT6A gene in a child with severe aplastic anemia
3个月前
已完结
Speech and language development and genotype–phenotype correlation in 49 individuals with KAT6A syndrome
6个月前
已完结
MOZ fusion proteins in acute myeloid leukaemia
6个月前
已完结
Serum Levels of Interleukins in Endometriosis Patients: A Systematic Review and Meta-analysis
7个月前
已完结
A novel pathogenic variant inOFD1results in X‐linked Joubert syndrome with orofaciodigital features and pituitary aplasia
7个月前
已完结
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