Lv31
250 积分 2023-11-27 加入
Clinical exome sequencing findings in 1589 patients
2个月前
已完结
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency
3个月前
已完结
[Analysis of a pyruvate kinase deficiency consanguineous pedigree caused by Ile314Thr homozygous mutation]
3个月前
已关闭
Investigation of GALNS variants and genotype–phenotype correlations in a large cohort of patients with mucopolysaccharidosis type IVA
3个月前
已完结
Incorporating second-tier genetic screening for multiple acyl-CoA dehydrogenase deficiency
3个月前
已完结
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