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PUBMED FOR HANDHELDS

Journal Abstract Search

214 related items for PubMed ID: 34050715

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  • 2. A Duplication Upstream of SOX9 Associated with SRY Negative 46,XX Ovotesticular Disorder of Sex Development: A Case Report.
    Mengen E, Kayhan G, Kocaay P, Uçaktürk SA.
    J Clin Res Pediatr Endocrinol; 2020 Sep 02; 12(3):308-314. PubMed ID: 31476840
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  • 3. Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.
    Seeherunvong T, Ukarapong S, McElreavey K, Berkovitz GD, Perera EM.
    J Pediatr Endocrinol Metab; 2012 Sep 02; 25(1-2):121-3. PubMed ID: 22570960
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  • 4. Duplication of SOX9 associated with 46,XX ovotesticular disorder of sex development.
    López-Hernández B, Méndez JP, Coral-Vázquez RM, Benítez-Granados J, Zenteno JC, Villegas-Ruiz V, Calzada-León R, Soderlund D, Canto P.
    Reprod Biomed Online; 2018 Jul 02; 37(1):107-112. PubMed ID: 29673731
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  • 6. Copy number variation in the region harboring SOX9 gene in dogs with testicular/ovotesticular disorder of sex development (78,XX; SRY-negative).
    Marcinkowska-Swojak M, Szczerbal I, Pausch H, Nowacka-Woszuk J, Flisikowski K, Dzimira S, Nizanski W, Payan-Carreira R, Fries R, Kozlowski P, Switonski M.
    Sci Rep; 2015 Oct 01; 5():14696. PubMed ID: 26423656
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  • 8. RevSex duplication-induced and sex-related differences in the SOX9 regulatory region chromatin landscape in human fibroblasts.
    Lybæk H, de Bruijn D, den Engelsman-van Dijk AH, Vanichkina D, Nepal C, Brendehaug A, Houge G.
    Epigenetics; 2014 Mar 01; 9(3):416-27. PubMed ID: 24351654
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  • 10. A 46,XX Ovotesticular Disorder of Sex Development Likely Caused by a Steroidogenic Factor-1 (NR5A1) Variant.
    Swartz JM, Ciarlo R, Guo MH, Abrha A, Weaver B, Diamond DA, Chan YM, Hirschhorn JN.
    Horm Res Paediatr; 2017 Mar 01; 87(3):191-195. PubMed ID: 27855412
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  • 13. Refining the regulatory region upstream of SOX9 associated with 46,XX testicular disorders of Sex Development (DSD).
    Hyon C, Chantot-Bastaraud S, Harbuz R, Bhouri R, Perrot N, Peycelon M, Sibony M, Rojo S, Piguel X, Bilan F, Gilbert-Dussardier B, Kitzis A, McElreavey K, Siffroi JP, Bashamboo A.
    Am J Med Genet A; 2015 Aug 01; 167A(8):1851-8. PubMed ID: 25900885
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  • 15. SOX3 duplication in a boy with 46,XX ovotesticular disorder of sex development and his 46,XX sister with atypical genitalia: Probable germline mosaicism.
    de Oliveira FM, Barros BA, Dos Santos AP, Campos NLV, Mazzola TN, Filho PL, Andrade LALA, Guaragna MS, de Mello MP, Guerra-Junior G, Vieira TAP, Maciel-Guerra AT.
    Am J Med Genet A; 2023 Feb 01; 191(2):592-598. PubMed ID: 36416214
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  • 16. Association between polymorphisms in the SOX9 region and canine disorder of sex development (78,XX; SRY-negative) revisited in a multibreed case-control study.
    Nowacka-Woszuk J, Szczerbal I, Stachowiak M, Szydlowski M, Nizanski W, Dzimira S, Maslak A, Payan-Carreira R, Wydooghe E, Nowak T, Switonski M.
    PLoS One; 2019 Feb 01; 14(6):e0218565. PubMed ID: 31220175
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  • 19. Diagnosis and management of non-CAH 46,XX disorders/differences in sex development.
    Yavas Abalı Z, Guran T.
    Front Endocrinol (Lausanne); 2024 Feb 01; 15():1354759. PubMed ID: 38812815
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  • 20. 46,XX ovotesticular DSD associated with a SOX3 gene duplication in a SRY-negative boy.
    Grinspon RP, Nevado J, Mori Alvarez Mde L, Del Rey G, Castera R, Venara M, Chiesa A, Podestá M, Lapunzina P, Rey RA.
    Clin Endocrinol (Oxf); 2016 Oct 01; 85(4):673-5. PubMed ID: 27260338
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