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60 积分 2024-06-26 加入
Comprehensive Review of Osteogenesis Imperfecta: Current Treatments and Future Innovations
1天前
已完结
Neurological Symptoms, Genotype-Phenotype Correlations and Ethnic-specific Differences in Bulgarian Patients With Wilson Disease
14天前
已完结
Newborn genetic screening for hearing impairment: a population-based longitudinal study
14天前
已完结
Variant frequency of GJB2 c.109G>A (p.Val37Ile) in the general Chinese population: A systematic review and meta-analysis
14天前
已关闭
Clinical implications of expanded carrier screening for pregnancy-related care and individual health
15天前
已关闭
Diagnosis and treatment of Friedreich ataxia: a European perspective
1个月前
已完结
Protection Provided by Cyclosporin A against Excitotoxic Neuronal Death Is Genotype Dependent
1个月前
已完结
HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families
2个月前
已完结
Genetic overview of postaxial polydactyly: Updated classification
3个月前
已完结
Classifications of Patterned Hair Loss
4个月前
已关闭
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