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3. Treatment management during the adolescent transition period of girls and young women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS): a systematic literature review. Wagner A; Brucker SY; Ueding E; Gröber-Grätz D; Simoes E; Rall K; Kronenthaler A; Schäffeler N; Rieger MA Orphanet J Rare Dis; 2016 Nov; 11(1):152. PubMed ID: 27852280 [TBL] [Abstract][Full Text] [Related]
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5. Development of a provisional model to improve transitional care for female adolescents with a rare genital malformation as an example for orphan diseases. Simoes E; Kronenthaler A; Emrich C; Rieger MA; Rall KK; Schäffeler N; Hiltner H; Ueding E; Brucker SY Biomed Res Int; 2014; 2014():913842. PubMed ID: 25544945 [TBL] [Abstract][Full Text] [Related]
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9. Mutations in WNT9B are associated with Mayer-Rokitansky-Küster-Hauser syndrome. Waschk DE; Tewes AC; Römer T; Hucke J; Kapczuk K; Schippert C; Hillemanns P; Wieacker P; Ledig S Clin Genet; 2016 May; 89(5):590-6. PubMed ID: 26610373 [TBL] [Abstract][Full Text] [Related]
10. Sexual activity of women with Mayer-Rokitansky-Küster-Hauser syndrome (MRKHS)--preliminary study. Beisert M; Szymañska-Pytlińska M; Kapczuk K; Chodeckal A; Walczyk-Matyja K; Kędzia W Ginekol Pol; 2015 Sep; 86(9):648-52. PubMed ID: 26665564 [TBL] [Abstract][Full Text] [Related]
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