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Journal Abstract Search

343 related items for PubMed ID: 24975471

  • 1. Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome: a case report and review of the literature.
    Herlin M, Højland AT, Petersen MB.
    Am J Med Genet A; 2014 Sep; 164A(9):2276-86. PubMed ID: 24975471
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  • 2. Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature.
    Bjørsum-Meyer T, Herlin M, Qvist N, Petersen MB.
    J Med Case Rep; 2016 Dec 21; 10(1):374. PubMed ID: 28003020
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  • 5. GREB1L as a candidate gene of Mayer-Rokitansky-Küster-Hauser Syndrome.
    Kyei Barffour I, Kyei Baah Kwarkoh R.
    Eur J Med Genet; 2021 Mar 21; 64(3):104158. PubMed ID: 33548512
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  • 11. Prevalence of urinary, prolapse, and bowel symptoms in Mayer-Rokitansky-Küster-Hauser syndrome.
    Pennesi CM, English EM, Bell S, Lossie AC, Quint EH, Swenson CW.
    Am J Obstet Gynecol; 2021 Jul 21; 225(1):70.e1-70.e12. PubMed ID: 33621544
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  • 12. Mayer-Rokitansky-Küster-Hauser syndrome with a uterine cervix and normal vagina associated with gonadal dysgenesis in a 46,XX female.
    Kisu I, Ono A, Iijma T, Katayama M, Iura A, Hirao N.
    J Obstet Gynaecol Res; 2019 Jul 21; 45(7):1386-1390. PubMed ID: 30912224
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  • 13. Prevalence and patient characteristics of Mayer-Rokitansky-Küster-Hauser syndrome: a nationwide registry-based study.
    Herlin M, Bjørn AM, Rasmussen M, Trolle B, Petersen MB.
    Hum Reprod; 2016 Oct 21; 31(10):2384-90. PubMed ID: 27609979
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  • 16. [Mayer-Rokitansky-Küster-Hauser syndrome].
    Herlin M, Petersen MB.
    Ugeskr Laeger; 2017 Mar 27; 179(13):. PubMed ID: 28397650
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  • 18. Inguinal ovary as a rare diagnostic sign of Mayer-Rokitansky-Küster-Hauser syndrome.
    Demirel F, Kara O, Esen I.
    J Pediatr Endocrinol Metab; 2012 Mar 27; 25(3-4):383-6. PubMed ID: 22768675
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