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.
ArticleOrphanet journal of rare diseases2026
Ewa Błaszczyk et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.