Lv1
30 积分 2022-11-02 加入
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
1个月前
已完结
Polymorphic CGG repeats in gene regulation and disease
1个月前
已完结
Carrier Detection in X‐Linked Mental Retardation
1个月前
已关闭
Fragile Sites on Human Chromosomes: Demonstration of Their Dependence on the Type of Tissue Culture Medium
1个月前
已完结
The fragile X chromosome
1个月前
已关闭
Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II
1个月前
已完结
De Novo SLC12A2 Variant Presenting as Congenital Hearing Loss With Vestibular Areflexia
1个月前
已完结
Improving the accuracy of noninvasive prenatal testing through size‐selection between fetal and maternal cfDNA
9个月前
已完结
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