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50 积分 2021-12-09 加入
Dysfibrinogenemia and hypofibrinogenemia - Spectrum of pathogenic variants in Slovak patients
4个月前
已完结
[Prenatal genetic diagnosis for two Chinese families affected with oculocutaneous albinism type Ⅱ]
7个月前
已完结
Genotype/phenotype correlation in 325 individuals referred for a diagnosis of tuberous sclerosis complex in the United States
11个月前
已关闭
Approaches for diagnosis and treatment in neurotransmitter disorders of childhood
1年前
已完结
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