Related Articles
First documented case of Myhre syndrome in Romania: A case report
Further phenotypic features and two novel <em>POC1A</em> variants in a patient with SOFT syndrome: A case report
Identification of a novel pathogenic <em>COL4A3</em> gene mutation in a Chinese family with autosomal dominant Alport syndrome: A case report
Sporadic pediatric severe familial adenomatous polyposis: A case report
Whole‑exome sequencing for high‑risk primary prostatic extra‑gastrointestinal stromal tumor: A case report