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Prenatal Diagnosis of Osteogenesis Imperfecta Type III
1个月前
已完结
Prevalence of C282Y, H63D, and S65C mutations in hereditary HFE-hemochromatosis gene in Lithuanian population
8个月前
已完结
Advances in haplotype phasing and genotype imputation
8个月前
已完结
Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles
10个月前
已完结
Activation of Imprinted Gene PW1 Promotes Cardiac Fibrosis After Ischemic Injury
10个月前
已完结
Imprinting disorders
10个月前
已完结
YARS1 Deficiency
11个月前
已关闭
Genome Organization, Function, and Imprinting in Prader-Willi and Angelman Syndromes
11个月前
已完结
The road to 11th edition of the International Classification of Diseases
1年前
已关闭
Participation and Intellectual Disability: A Review of the Literature
1年前
已关闭
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