Related Articles
1q21.1 microduplication in a patient with mental impairment and congenital heart defect
Targeted next‑generation sequencing for research and diagnostics in congenital heart disease, and cleft lip and/or palate
A clinical and molecular analysis of a patient with Emanuel syndrome
Hypospadias in a male infant with an unusual mosaic 45,X/46,X,psu idic(Y)(p11.32)/46,XY and haploinsufficiency of SHOX: A case report
Microduplication of 7q36.3 encompassing the SHH long‑range regulator (ZRS) in a patient with triphalangeal thumb‑polysyndactyly syndrome and congenital heart disease