Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.
published in: Orphanet Journal of Rare Diseases
date of publication: 2009-11-04
main subject: Müllerian agenesis
Cites articles 21
- 1999-12-01
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Article - wd:Q37422356