166 related articles for article (PubMed ID: 30739119)
1. Sequence Variants in TBX6 Are Associated with Disorders of the Müllerian Ducts: An Update.
Tewes AC; Hucke J; Römer T; Kapczuk K; Schippert C; Hillemanns P; Wieacker P; Ledig S
Sex Dev; 2019; 13(1):35-40. PubMed ID: 30739119
[TBL] [Abstract][Full Text] [Related]
2. Variations in RBM8A and TBX6 are associated with disorders of the müllerian ducts.
Tewes AC; Rall KK; Römer T; Hucke J; Kapczuk K; Brucker S; Wieacker P; Ledig S
Fertil Steril; 2015 May; 103(5):1313-8. PubMed ID: 25813282
[TBL] [Abstract][Full Text] [Related]
3. Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
Chen N; Zhao S; Jolly A; Wang L; Pan H; Yuan J; Chen S; Koch A; Ma C; Tian W; Jia Z; Kang J; Zhao L; Qin C; Fan X; Rall K; Coban-Akdemir Z; Chen Z; Jhangiani S; Liang Z; Niu Y; Li X; Yan Z; Wu Y; Dong S; Song C; Qiu G; Zhang S; Liu P; Posey JE; Zhang F; Luo G; Wu Z; ; Su J; Zhang J; Chen EY; Rouskas K; Glentis S; Bacopoulou F; Deligeoroglou E; Chrousos G; Lyonnet S; Polak M; Rosenberg C; Dingeldein I; Bonilla X; Borel C; Gibbs RA; Dietrich JE; Dimas AS; Antonarakis SE; Brucker SY; Lupski JR; Wu N; Zhu L
Am J Hum Genet; 2021 Feb; 108(2):337-345. PubMed ID: 33434492
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Functional characteristics of a broad spectrum of TBX6 variants in Mayer-Rokitansky-Küster-Hauser syndrome.
Ma C; Chen N; Jolly A; Zhao S; Coban-Akdemir Z; Tian W; Kang J; Ye Y; Wang Y; Koch A; Zhang Y; Qin C; Bonilla X; Borel C; Rall K; Chen Z; Jhangiani S; Niu Y; Li X; Qiu G; Zhang S; Luo G; Wu Z; Bacopoulou F; Deligeoroglou E; Zhang TJ; Rosenberg C; Gibbs RA; Dietrich JE; Dimas AS; Liu P; Antonarakis SE; Brucker SY; Posey JE; Lupski JR; Wu N; Zhu L;
Genet Med; 2022 Nov; 24(11):2262-2273. PubMed ID: 36112137
[TBL] [Abstract][Full Text] [Related]
6. TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia.
Sandbacka M; Laivuori H; Freitas É; Halttunen M; Jokimaa V; Morin-Papunen L; Rosenberg C; Aittomäki K
Orphanet J Rare Dis; 2013 Aug; 8():125. PubMed ID: 23954021
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Recurrent human 16p11.2 microdeletions in type I Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome patients in Chinese Han population.
Su K; Liu H; Ye X; Jin H; Xie Z; Yang C; Zhou D; Huang H; Wu Y
Mol Genet Genomic Med; 2024 Jan; 12(1):e2280. PubMed ID: 37789575
[TBL] [Abstract][Full Text] [Related]
9. Array-comparative genomic hybridization analysis in patients with Müllerian fusion anomalies.
Ledig S; Tewes AC; Hucke J; Römer T; Kapczuk K; Schippert C; Hillemanns P; Wieacker P
Clin Genet; 2018 Mar; 93(3):640-646. PubMed ID: 29068465
[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. 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]
12. GREB1L as a candidate gene of Mayer-Rokitansky-Küster-Hauser Syndrome.
Kyei Barffour I; Kyei Baah Kwarkoh R
Eur J Med Genet; 2021 Mar; 64(3):104158. PubMed ID: 33548512
[TBL] [Abstract][Full Text] [Related]
13. Variants in genes related to development of the urinary system are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Chu C; Li L; Li S; Zhou Q; Zheng P; Zhang YD; Duan AH; Lu D; Wu YM
Hum Genomics; 2022 Mar; 16(1):10. PubMed ID: 35361250
[TBL] [Abstract][Full Text] [Related]
14. Familial occurrence of Mayer-Rokitansky-Küster-Hauser syndrome.
Ma X; Yao B; Pan Q; Xu W; Xu K; Ma F
J Obstet Gynaecol; 2016 Aug; 36(6):817-818. PubMed ID: 27150594
[No Abstract] [Full Text] [Related]
15. Mayer-Rokitansky-Küster-Hauser syndrome: two case reports.
Sánchez Malo MJ; Arrudi Moreno M; de Arriba Muñoz A
Med Clin (Barc); 2018 Jul; 151(2):e9-e10. PubMed ID: 29292105
[No Abstract] [Full Text] [Related]
16. Mayer-Rokitansky-Künster-Hauser syndrome due to 2q12.1q14.1 deletion: PAX8 the causing gene?
Smol T; Ribero-Karrouz W; Edery P; Gorduza DB; Catteau-Jonard S; Manouvrier-Hanu S; Ghoumid J
Eur J Med Genet; 2020 Apr; 63(4):103812. PubMed ID: 31731040
[TBL] [Abstract][Full Text] [Related]
17. Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion region are associated with Mayer-Rokitansky-Kuster Hauser (MRKH) syndrome.
Brakta S; Du Q; Chorich LP; Hawkins ZA; Sullivan ME; Ko EK; Kim HG; Knight J; Taylor HS; Friez M; Phillips JA; Layman LC
Mol Cell Endocrinol; 2024 Aug; 589():112237. PubMed ID: 38599276
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: a historical perspective.
Patnaik SS; Brazile B; Dandolu V; Ryan PL; Liao J
Gene; 2015 Jan; 555(1):33-40. PubMed ID: 25260227
[TBL] [Abstract][Full Text] [Related]
20. Sequence variants in ESR1 and OXTR are associated with Mayer-Rokitansky-Küster-Hauser syndrome.
Brucker SY; Frank L; Eisenbeis S; Henes M; Wallwiener D; Riess O; van Eijck B; Schöller D; Bonin M; Rall KK
Acta Obstet Gynecol Scand; 2017 Nov; 96(11):1338-1346. PubMed ID: 28815558
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
