BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

619 related articles for article (PubMed ID: 19852431)

  • 1. Analysis of the SRY gene in a girl with 45,X/46,XY genotype.
    Akbas E; Soylemez F; Hallioglu O; Polat S; Turkoz G
    Genet Couns; 2009; 20(3):249-54. PubMed ID: 19852431
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mixed gonadal dysgenesis with 45,X/46,X,idic(Y)/46,XY,idic(Y) karyotype.
    Caglayan AO; Demiryilmaz F; Kendirci M; Ozyazgan I; Akalin H; Bittmann S
    Genet Couns; 2009; 20(2):173-9. PubMed ID: 19650415
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gonadal mosaicism 45,X/46,X,psu dic(Y)(q11.2) resulting in a Turner phenotype with mixed gonadal dysgenesis.
    Gole LA; Lim J; Crolla JA; Loke KY
    Singapore Med J; 2008 Apr; 49(4):349-51. PubMed ID: 18418530
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Y chromosome structural abnormalities and Turner's syndrome].
    Ravel C; Siffroi JP
    Gynecol Obstet Fertil; 2009 Jun; 37(6):511-8. PubMed ID: 19464936
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.
    Bergendi E; Plöchl E; Vlasak I; Rittinger O; Muss W
    Klin Padiatr; 1997; 209(3):133-6. PubMed ID: 9183775
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.
    Daggag H; Srour W; El-Khateeb M; Ajlouni K
    Sex Dev; 2013; 7(6):295-302. PubMed ID: 23988405
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A point mutation, R59G, within the HMG-SRY box in a female 45,X/46,X, psu dic(Y)(pter-->q11::q11-->pter).
    Fernandez R; Marchal JA; Sanchez A; Pasaro E
    Hum Genet; 2002 Sep; 111(3):242-6. PubMed ID: 12215836
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Epigenetic abnormality of SRY gene in the adult XY female with pericentric inversion of the Y chromosome.
    Mitsuhashi T; Warita K; Sugawara T; Tabuchi Y; Takasaki I; Kondo T; Hayashi F; Wang ZY; Matsumoto Y; Miki T; Takeuchi Y; Ebina Y; Yamada H; Sakuragi N; Yokoyama T; Nanmori T; Kitagawa H; Kant JA; Hoshi N
    Congenit Anom (Kyoto); 2010 Jun; 50(2):85-94. PubMed ID: 20184645
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
    Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Familial Turner syndrome with an X;Y translocation mosaicism: implications for genetic counseling.
    Portnoï MF; Chantot-Bastaraud S; Christin-Maitre S; Carbonne B; Beaujard MP; Keren B; Lévy J; Dommergues M; Cabrol S; Hyon C; Siffroi JP
    Eur J Med Genet; 2012 Nov; 55(11):635-40. PubMed ID: 22809487
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Turner syndrome and 45,X/47,XXX mosaicism.
    Akbas E; Mutluhan H; Savasoglu K; Soylemez F; Ozturk I; Yazici G
    Genet Couns; 2009; 20(2):141-6. PubMed ID: 19650411
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Axenfeld-Rieger spectrum in a patient with 45,X Turner syndrome.
    Abdalla EM; Nabil KM
    Ophthalmic Genet; 2012 Jun; 33(2):111-5. PubMed ID: 22229795
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Gonadoblastoma in patients with Ullrich-Turner syndrome.
    Zelaya G; López Marti JM; Marino R; Garcia de Dávila MT; Gallego MS
    Pediatr Dev Pathol; 2015; 18(2):117-21. PubMed ID: 25535833
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development.
    Brambila-Tapia AJ; Rivera H; García-Castillo H; Domínguez-Quezada MG; Dávalos-Rodríguez IP
    Fertil Steril; 2009 Nov; 92(5):1747.e5-7. PubMed ID: 19732877
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sex chromosome mosaicism of X/XY or X/XY/XYY.
    Wilson MG; Ebbin AJ; Shinno NW; Towner JW
    Birth Defects Orig Artic Ser; 1975; 11(5):255-66. PubMed ID: 1218222
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [45,X/46, XYnf/47, XYnfYnf/46, X, dic (Ynf) (q12) mosaicism in a female patient with gonadal dysgenesis and the stigmata of Turner's syndrome].
    Gil R; Galán F; López-Ginés C; Gregori-Romero M; Millet A; Pellín A; Llombart-Bosch A
    Rev Clin Esp; 1991 Jun; 189(1):23-5. PubMed ID: 1924922
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The role of SRY mutations in the etiology of gonadal dysgenesis in patients with 45,X/46,XY disorder of sex development and variants.
    Nishi MY; Costa EM; Oliveira SB; Mendonca BB; Domenice S
    Horm Res Paediatr; 2011; 75(1):26-31. PubMed ID: 20699606
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Short stature in patients with 45,X/46,XY mosaicism: report of three cases.
    Lee CF; Su PH; Chen JY; Chen SJ; Yang KC; Lin LL
    Acta Paediatr Taiwan; 2006; 47(6):312-6. PubMed ID: 17407984
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
    Reshmi SC; Miller JL; Deplewski D; Close C; Henderson LJ; Littlejohn E; Schwartz S; Waggoner DJ
    Eur J Med Genet; 2011; 54(2):161-4. PubMed ID: 21078420
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genotypic sex and phenotypic sex: clinical, biochemical and molecular aspects in a patient with male hypogonadism and 46XX-45XO karyotype].
    Torre R; Savino A; Venturi P; Taverna R; Triacca R; Coli A; Bernasconi D; Del Monte P; Marugo M
    Recenti Prog Med; 2001 Dec; 92(12):747-50. PubMed ID: 11822095
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 31.