Related Articles
Clinical characteristics and phenotype distribution in 10 Chinese patients with X‑linked adrenoleukodystrophy
A frameshift mutation in the CHM gene causes choroideremia with acute angle‑closure glaucoma
X chromosome inactivation in human parthenogenetic embryonic stem cells following prolonged passaging
Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results
Global analysis of chromosome X gene expression in primary cultures of normal ovarian surface epithelial cells and epithelial ovarian cancer cell lines