Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report

Morten K Herlin, Vang Q Le, H Allan T, Anja Ernst, Henrik Okkels, Astrid C Petersen, Michael B Petersen, Inge S Pedersen

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

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