Related Articles
De novo unbalanced translocation t(15;22)(q26.2;q12) with velo‑cardio‑facial syndrome: A case report and review of the literature
A twin sibling with Prader-Willi syndrome caused by type 2 microdeletion following assisted reproductive technology: A case report
<em>De novo</em> 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case report
Application of an improved targeted next generation sequencing method to diagnose non‑syndromic mental retardation in one step: A case report
Detection of chromosomal abnormalities and the 22q11 microdeletion in fetuses with congenital heart defects