Lv34
220 积分 2023-08-31 加入
Progress of newborn screening in China
5小时前
已完结
Glycogen storage diseases
10小时前
已完结
糖原累积病Ⅰa型的诊断 治疗和预防专家共识
2天前
已完结
The Endocrine Chameleon: Expanding the phenotype of Pseudohypoparathyroidism 1A in infancy
2天前
求助中
Heterozygous Missense Mutations in Steroidogenic Factor 1 (SF1/Ad4BP, NR5A1) Are Associated with 46,XY Disorders of Sex Development with Normal Adrenal Function
16天前
已关闭
Genetic and Clinical Characteristics of 185 Japanese Children with 46,XY Differences of Sex Development
2个月前
已关闭
Genetic and Clinical Characteristics of 185 Japanese Children with 46,XY Differences of Sex Development
2个月前
已关闭
Madelung Deformity
3个月前
已完结
Radiological Signs of Leri-Weill Dyschondrosteosis in Turner Syndrome
3个月前
已关闭
Mutations inProkineticin 2andProkineticin receptor 2genes in Human Gonadotrophin-Releasing Hormone Deficiency: Molecular Genetics and Clinical Spectrum
3个月前
已完结
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