Related Articles
Molecular cytogenetic characterization of partial monosomy 2p and trisomy 16q in a newborn: A case report
A duplication upstream of SOX9 was not positively correlated with the SRY‑negative 46,XX testicular disorder of sex development: A case report and literature review
Partial monosomy 8p and trisomy 16q in two children with developmental delay detected by array comparative genomic hybridization
Turner syndrome caused by rare complex structural abnormalities involving chromosome X
Rare de novo inversion-duplication case with pure 3qter duplication syndrome including an overlap of the dup(3q) critical region: A case report