161 related articles for article (PubMed ID: 22503279)
1. Mutations in WNT4 are not responsible for Müllerian duct abnormalities in Chinese women.
Chang X; Qin Y; Xu C; Li G; Zhao X; Chen ZJ
Reprod Biomed Online; 2012 Jun; 24(6):630-3. PubMed ID: 22503279
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).
Philibert P; Biason-Lauber A; Gueorguieva I; Stuckens C; Pienkowski C; Lebon-Labich B; Paris F; Sultan C
Fertil Steril; 2011 Jun; 95(8):2683-6. PubMed ID: 21377155
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.
Williams LS; Demir Eksi D; Shen Y; Lossie AC; Chorich LP; Sullivan ME; Phillips JA; Erman M; Kim HG; Alper OM; Layman LC
Fertil Steril; 2017 Jul; 108(1):145-151.e2. PubMed ID: 28600106
[TBL] [Abstract][Full Text] [Related]
7. Absence of WNT4 gene mutation in a patient with MURCS association.
Shoar Z; Ganguly T; Anderson CE; De Luca F; Suarez E
J Pediatr Endocrinol Metab; 2014 May; 27(5-6):555-9. PubMed ID: 24356390
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia.
Nik-Zainal S; Strick R; Storer M; Huang N; Rad R; Willatt L; Fitzgerald T; Martin V; Sandford R; Carter NP; Janecke AR; Renner SP; Oppelt PG; Oppelt P; Schulze C; Brucker S; Hurles M; Beckmann MW; Strissel PL; Shaw-Smith C
J Med Genet; 2011 Mar; 48(3):197-204. PubMed ID: 21278390
[TBL] [Abstract][Full Text] [Related]
10. Analysis of WNT9B mutations in Chinese women with Mayer-Rokitansky-Küster-Hauser syndrome.
Wang M; Li Y; Ma W; Li H; He F; Pu D; Su T; Wang S
Reprod Biomed Online; 2014 Jan; 28(1):80-5. PubMed ID: 24268733
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Laparoscopic evaluation of pelvic pain with Surgicel vaginoplasty in a woman with Mayer Rokitansky Kuster Hauser syndrome.
Deka D; Gupta N; Dadhwal V; Mittal S
Eur J Obstet Gynecol Reprod Biol; 2011 Jan; 154(1):115-6. PubMed ID: 20728979
[No Abstract] [Full Text] [Related]
14. 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]
15. Mutation analysis of WNT4 gene in SRY negative 46,XX DSD patients with Mullerian agenesis and/or gonadal dysgenesis- An Indian study.
Ragitha TS; Sunish KS; Gilvaz S; Daniel S; Varghese PR; Raj S; Francis J; Suresh Kumar R
Gene; 2023 Apr; 861():147236. PubMed ID: 36738897
[TBL] [Abstract][Full Text] [Related]
16. Mutational analysis of the WNT gene family in women with Mayer-Rokitansky-Kuster-Hauser syndrome.
Ravel C; Lorenço D; Dessolle L; Mandelbaum J; McElreavey K; Darai E; Siffroi JP
Fertil Steril; 2009 Apr; 91(4 Suppl):1604-7. PubMed ID: 19171330
[TBL] [Abstract][Full Text] [Related]
17. Müllerian remnant leiomyomas in women with Mayer-Rokitansky-Küster-Hauser syndrome.
Fletcher HM; Campbell-Simpson K; Walcott D; Harriott J
Obstet Gynecol; 2012 Feb; 119(2 Pt 2):483-485. PubMed ID: 22270447
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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]
[Next] [New Search]
