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Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Morcel K, Camborieux L; Programme de Recherches sur les Aplasies Müllériennes; Guerrier D. Morcel K, et al. Among authors: guerrier d. Orphanet J Rare Dis. 2007 Mar 14;2:13. doi: 10.1186/1750-1172-2-13. Orphanet J Rare Dis. 2007. PMID: 17359527 Free PMC article. Review.
Phenotypic variability of a 4q34-->qter inherited deletion: MRKH syndrome in the daughter, cardiac defect and Fallopian tube cancer in the mother.
Bendavid C, Pasquier L, Watrin T, Morcel K, Lucas J, Gicquel I, Dubourg C, Henry C, David V, Odent S, Levêque J, Pellerin I, Guerrier D. Bendavid C, et al. Among authors: guerrier d. Eur J Med Genet. 2007 Jan-Feb;50(1):66-72. doi: 10.1016/j.ejmg.2006.09.003. Epub 2006 Oct 1. Eur J Med Genet. 2007. PMID: 17081814
Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome.
Morcel K, Dallapiccola B, Pasquier L, Watrin T, Bernardini L, Guerrier D. Morcel K, et al. Among authors: guerrier d. Eur J Hum Genet. 2012 Feb;20(2). doi: 10.1038/ejhg.2011.158. Epub 2011 Sep 7. Eur J Hum Genet. 2012. PMID: 21897448 Free PMC article. No abstract available.
53 results