Lv1
50 积分 2023-06-14 加入
Hereditary chronic neutrophilic leukemia in a four‐generation family without transformation to acute leukemia
5个月前
已完结
Comprehensive analysis of chromosome abnormalities by chromosome conformation based karyotyping (C-MoKa) in patients with conception failure and pregnancy loss
6个月前
已完结
人类基因变异的命名规则
8个月前
已完结
Phenotyping and genotyping inherited retina]diseases: Molecular genetics, clinical and imagingfeatures,and therapeutics of macular dystrophiescone and cone-rod dystrophies,rod-conedystrophies,Leber congenital amaurosis,and conedysfunction syndromes
11个月前
已完结
The expanding diagnostic toolbox for rare geneticdiseases
11个月前
已完结
Phenvlalanine hvdroxylase deficiency diagnosis andmanagement:A 2023 evidence-based clinicalquideline of the American College of Medical Geneticsand Genomics(ACMG)
11个月前
已关闭
针对生育人群的携带者筛查实验室和临床实践专家共识
11个月前
已完结
孕前及孕早期常见隐性单基因遗传病携带者筛查临床应用专家共识
11个月前
已完结
[Sperm-fluorescence in situ hybridization analysis in patients with pericentric inversions of Y chromosome]
1年前
已关闭
State of the Art for Genetic Testing of Infertile Men
1年前
已完结
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