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 tidsskriftTidsskriftartikelForskningpeer review

33 Citationer (Scopus)

Fingeraftryk

Dyk ned i forskningsemnerne om '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'. Sammen danner de et unikt fingeraftryk.

Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology

Immunology and Microbiology