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20 积分 2026-03-03 加入
Subtelomeric deletions of chromosome 6p: molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome
15天前
已完结
Partial duplication of 4q12q13 leads to a mild phenotype
1个月前
已完结
A Rare de novo Interstitial Duplication at 4p15.2 in a Boy with Severe Congenital Heart Defects, Limb Anomalies, Hypogonadism, and Global Developmental Delay
5个月前
已完结