Search for altered imprinting marks in Mayer–Rokitansky–Küster–Hauser patients

BACKGROUND: Mayer–Rokitansky–Küster–Hauser syndrome (MRKH) is the second most common cause of primary amenorrhea and characterized by absence of the uterus and the upper part of the vagina. The etiology of MRKH is mainly unknown but a contribution of genomic alterations is probable. A molecular dist...

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Bibliografiske detaljer
Udgivet i:Mol Genet Genomic Med
Main Authors: Eggermann, Thomas, Ledig, Susanne, Begemann, Matthias, Elbracht, Miriam, Kurth, Ingo, Wieacker, Peter
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2018
Fag:
Clinical Reports
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6305658/
https://ncbi.nlm.nih.gov/pubmed/30099855
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.426
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