← Evidence map

ArticleOrphanet journal of rare diseases2026

Refining the diagnosis of 46,XY disorders of sex development: insight from whole-exome sequencing.

Ewa Błaszczyk et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

Not cited yet

Full record →Abstract, authors, funding and every citing paper · PMID 42365275