BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 35883945)

  • 1. Identification of Genetic Causes in Mayer-Rokitansky-Küster-Hauser (MRKH) Syndrome: A Systematic Review of the Literature.
    Triantafyllidi VE; Mavrogianni D; Kalampalikis A; Litos M; Roidi S; Michala L
    Children (Basel); 2022 Jun; 9(7):. PubMed ID: 35883945
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome: advancements and implications.
    Herlin MK
    Front Endocrinol (Lausanne); 2024; 15():1368990. PubMed ID: 38699388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and genetic aspects of Mayer-Rokitansky-Küster-Hauser syndrome.
    Ledig S; Wieacker P
    Med Genet; 2018; 30(1):3-11. PubMed ID: 29527097
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The genetics of Mullerian aplasia.
    Layman LC
    Expert Rev Endocrinol Metab; 2014 Jul; 9(4):411-419. PubMed ID: 30763999
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional genomics analysis identifies loss of HNF1B function as a cause of Mayer-Rokitansky-Küster-Hauser syndrome.
    Thomson E; Tran M; Robevska G; Ayers K; van der Bergen J; Gopalakrishnan Bhaskaran P; Haan E; Cereghini S; Vash-Margita A; Margetts M; Hensley A; Nguyen Q; Sinclair A; Koopman P; Pelosi E
    Hum Mol Genet; 2023 Mar; 32(6):1032-1047. PubMed ID: 36282544
    [TBL] [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. 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. Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report.
    Dell'Edera D; Allegretti A; Ventura M; Mercuri L; Mitidieri A; Cuscianna G; Epifania AA; Morizio E; Alfonsi M; Guanciali-Franchi P
    J Med Case Rep; 2021 Apr; 15(1):208. PubMed ID: 33883018
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Recurrent aberrations identified by array-CGH in patients with Mayer-Rokitansky-Küster-Hauser syndrome.
    Ledig S; Schippert C; Strick R; Beckmann MW; Oppelt PG; Wieacker P
    Fertil Steril; 2011 Apr; 95(5):1589-94. PubMed ID: 20797712
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Syndrome Mayer-Rokitansky-Küster-Hauser - uterine and vaginal agenesis: current knowledge and therapeutic options.
    Chmel R; Pastor Z; Mužík M; Brtnický T; Nováčková M
    Ceska Gynekol; 2019; 84(5):386-392. PubMed ID: 31826637
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. Recurrent microdeletion at 17q12 as a cause of Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome: two case reports.
    Bernardini L; Gimelli S; Gervasini C; Carella M; Baban A; Frontino G; Barbano G; Divizia MT; Fedele L; Novelli A; Béna F; Lalatta F; Miozzo M; Dallapiccola B
    Orphanet J Rare Dis; 2009 Nov; 4():25. PubMed ID: 19889212
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Place of ultrasound in the management of Mayer-Rokitansky-Kuster-Hauser syndrome. Observational study from 2000 to 2017 within university hospital of Strasbourg].
    Schwaab T; Bryand A
    Gynecol Obstet Fertil Senol; 2019 Nov; 47(11):783-789. PubMed ID: 31280033
    [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. Importance of Laparoscopic Assessment of the Uterine Adnexa in a Mayer-Rokitansky-Kuster-Hauser Syndrome Type II Case.
    Dragusin R; Tudorache Ș; Surlin V; Lichiardopol C; Iliescu DG
    Curr Health Sci J; 2014; 40(2):144-7. PubMed ID: 25729598
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 225(1):70.e1-70.e12. PubMed ID: 33621544
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 15.