Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome: A case report and review of the literature
Author:
Affiliation:
1. Department of Clinical Genetics; Aalborg University Hospital; Aalborg Denmark
2. Department of Clinical Medicine; Aalborg University; Aalborg Denmark
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36652/fullpdf
Reference69 articles.
1. Familial form of Rokitansky-Kuster-Hauser syndrome;Anger;Bull Fed Soc Gynecol Obstet Lang Fr,1966
2. Familial occurrence of hereditary renal adysplasia with Müllerian anomalies;Battin;Clin Genet,1993
3. Phenotypic variability of a 4q34→qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother;Bendavid;Eur J Med Genet,2007
4. Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: Two case reports;Bernadini;Orphanet J Rare Dis,2009
5. A WNT4 mutation associated with Müllerian-duct regression and virilization in a 46,XX woman;Biason-Lauber;New Engl J Med,2004
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