213 related articles for article (PubMed ID: 21619687)
1. A combination of transcriptome and methylation analyses reveals embryologically-relevant candidate genes in MRKH patients.
Rall K; Barresi G; Walter M; Poths S; Haebig K; Schaeferhoff K; Schoenfisch B; Riess O; Wallwiener D; Bonin M; Brucker S
Orphanet J Rare Dis; 2011 May; 6():32. PubMed ID: 21619687
[TBL] [Abstract][Full Text] [Related]
2. Utero-vaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome) associated with deletions in known DiGeorge or DiGeorge-like loci.
Morcel K; Watrin T; Pasquier L; Rochard L; Le Caignec C; Dubourg C; Loget P; Paniel BJ; Odent S; David V; Pellerin I; Bendavid C; Guerrier D
Orphanet J Rare Dis; 2011 Mar; 6():9. PubMed ID: 21406098
[TBL] [Abstract][Full Text] [Related]
3. Involvement of ITIH5, a candidate gene for congenital uterovaginal aplasia (Mayer-Rokitansky-Küster-Hauser syndrome), in female genital tract development.
Morcel K; Watrin T; Jaffre F; Deschamps S; Omilli F; Pellerin I; Levêque J; Guerrier D
Gene Expr; 2012; 15(5-6):207-14. PubMed ID: 23539898
[TBL] [Abstract][Full Text] [Related]
4. SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome.
Gervasini C; Grati FR; Lalatta F; Tabano S; Gentilin B; Colapietro P; De Toffol S; Frontino G; Motta F; Maitz S; Bernardini L; Dallapiccola B; Fedele L; Larizza L; Miozzo M
Genet Med; 2010 Oct; 12(10):634-40. PubMed ID: 20847698
[TBL] [Abstract][Full Text] [Related]
5. Gene expression profile of patients with Mayer-Rokitansky-Küster-Hauser syndrome: new insights into the potential role of developmental pathways.
Nodale C; Ceccarelli S; Giuliano M; Cammarota M; D'Amici S; Vescarelli E; Maffucci D; Bellati F; Panici PB; Romano F; Angeloni A; Marchese C
PLoS One; 2014; 9(3):e91010. PubMed ID: 24608967
[TBL] [Abstract][Full Text] [Related]
6. Mayer-Rokitansky-Kuster-Hauser syndrome diagnosed by magnetic resonance imaging. Role of imaging to identify and evaluate the uncommon variation in development of the female genital tract.
Fiaschetti V; Taglieri A; Gisone V; Coco I; Simonetti G
J Radiol Case Rep; 2012 Apr; 6(4):17-24. PubMed ID: 22690292
[TBL] [Abstract][Full Text] [Related]
7. Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome.
Fontana L; Gentilin B; Fedele L; Gervasini C; Miozzo M
Clin Genet; 2017 Feb; 91(2):233-246. PubMed ID: 27716927
[TBL] [Abstract][Full Text] [Related]
8. Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome.
Chen MJ; Wei SY; Yang WS; Wu TT; Li HY; Ho HN; Yang YS; Chen PL
Hum Reprod; 2015 Jul; 30(7):1732-42. PubMed ID: 25924657
[TBL] [Abstract][Full Text] [Related]
9. Inguinal ovary as a rare diagnostic sign of Mayer-Rokitansky-Küster-Hauser syndrome.
Demirel F; Kara O; Esen I
J Pediatr Endocrinol Metab; 2012; 25(3-4):383-6. PubMed ID: 22768675
[TBL] [Abstract][Full Text] [Related]
10. [Typical form of Mayer-Rokitansky-Küster-Hauser syndrome and ectopic kidney. A rare association].
El Khamlichi A; Allali N; Dafiri R
Gynecol Obstet Fertil; 2011 Feb; 39(2):e40-3. PubMed ID: 21288753
[TBL] [Abstract][Full Text] [Related]
11. Mullerian dysgenesis: a critical review of the literature.
Choussein S; Nasioudis D; Schizas D; Economopoulos KP
Arch Gynecol Obstet; 2017 Jun; 295(6):1369-1381. PubMed ID: 28434104
[TBL] [Abstract][Full Text] [Related]
12. Associations of Polymorphisms in WNT9B and PBX1 with Mayer-Rokitansky-Küster-Hauser Syndrome in Chinese Han.
Ma W; Li Y; Wang M; Li H; Su T; Li Y; Wang S
PLoS One; 2015; 10(6):e0130202. PubMed ID: 26075712
[TBL] [Abstract][Full Text] [Related]
13. Whole-exome sequencing identifies a GREB1L variant in a three-generation family with Müllerian and renal agenesis: a novel candidate gene in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome. A case report.
Herlin MK; Le VQ; Højland AT; Ernst A; Okkels H; Petersen AC; Petersen MB; Pedersen IS
Hum Reprod; 2019 Sep; 34(9):1838-1846. PubMed ID: 31424080
[TBL] [Abstract][Full Text] [Related]
14. A case of Mayer-Rokitansky-Küster-Hauser syndrome presenting as Graves disease.
Lim YJ; Sohn TS; Kang SH; Chang KY; Kim BK; Kim YJ; Ha WC; Oh SJ; Son HS
J Pediatr Endocrinol Metab; 2012; 25(11-12):1169-71. PubMed ID: 23329766
[TBL] [Abstract][Full Text] [Related]
15. [Mayer-Rokitansky-Küster-Hauser syndrome. A report of two cases].
Bautista-Gómez E; Morales-García V; Galván Espinosa H; Flores-Romero AL; Vásquez Santiago E; Pizarro Osorno N
Ginecol Obstet Mex; 2012 Oct; 80(10):663-7. PubMed ID: 23240231
[TBL] [Abstract][Full Text] [Related]
16. HOXA10 and HOXA13 sequence variations in human female genital malformations including congenital absence of the uterus and vagina.
Ekici AB; Strissel PL; Oppelt PG; Renner SP; Brucker S; Beckmann MW; Strick R
Gene; 2013 Apr; 518(2):267-72. PubMed ID: 23376215
[TBL] [Abstract][Full Text] [Related]
17. Frame shift mutation of LHX1 is associated with Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome.
Ledig S; Brucker S; Barresi G; Schomburg J; Rall K; Wieacker P
Hum Reprod; 2012 Sep; 27(9):2872-5. PubMed ID: 22740494
[TBL] [Abstract][Full Text] [Related]
18. Low prevalence of male microchimerism in women with Mayer-Rokitansky-Küster-Hauser syndrome.
Peters HE; Johnson BN; Ehli EA; Micha D; Verhoeven MO; Davies GE; Dekker JJML; Overbeek A; Berg MHVD; Dulmen-den Broeder EV; Leeuwen FEV; Mijatovic V; Boomsma DI; Lambalk CB
Hum Reprod; 2019 Jun; 34(6):1117-1125. PubMed ID: 31111890
[TBL] [Abstract][Full Text] [Related]
19. GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndrome.
Jacquinet A; Boujemla B; Fasquelle C; Thiry J; Josse C; Lumaka A; Brischoux-Boucher E; Dubourg C; David V; Pasquier L; Lehman A; Morcel K; Guerrier D; Bours V
Clin Genet; 2020 Aug; 98(2):126-137. PubMed ID: 32378186
[TBL] [Abstract][Full Text] [Related]
20. Clinical utility gene card for: Mayer-Rokitansky-Küster-Hauser syndrome.
Morcel K; Dallapiccola B; Pasquier L; Watrin T; Bernardini L; Guerrier D
Eur J Hum Genet; 2012 Feb; 20(2):. PubMed ID: 21897448
[No Abstract] [Full Text] [Related]
[Next] [New Search]
