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90 积分 2025-08-05 加入
Clinical, biochemical characteristics and genotype-phenotype analysis of congenital hypothyroidism diagnosed by newborn screening in China
1天前
已完结
Whole genome sequencing of apparently mutation-negative MEN1 patients
3个月前
已关闭
Analysis of clinical manifestation and a mosaic frameshift variant of the KMT2D gene in a Chinese patient with Kabuki syndrome
5个月前
已完结
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