These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

373 related articles for article (PubMed ID: 9783714)

  • 1. Discordant phenotypes and 45,X/46,X,idic(Y).
    Kelly TE; Franko JB; Rogol A; Golden WL
    J Med Genet; 1998 Oct; 35(10):862-4. PubMed ID: 9783714
    [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. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
    Aktas D; Alikasifoglu M; Gonc N; Senocak ME; Tuncbilek E
    Eur J Med Genet; 2006; 49(2):141-9. PubMed ID: 16530711
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cytogenetic and molecular characterization of two isodicentric Y chromosomes.
    Stankiewicz P; Hélias-Rodzewicz Z; Jakubów-Durska K; Bocian E; Obersztyn E; Rappold GA; Mazurczak T
    Am J Med Genet; 2001 Jun; 101(1):20-5. PubMed ID: 11343332
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 45,X/46,X,idic(Yq) mosaicism: clinical, cytogenetic, and molecular studies in four individuals.
    Teraoka M; Narahara K; Yokoyama Y; Tsuji K; Kikkawa K; Ito S; Koyama K; Seino Y
    Am J Med Genet; 1998 Aug; 78(5):424-8. PubMed ID: 9714008
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 45,X/46,XY mosaicism: report of 27 cases.
    Telvi L; Lebbar A; Del Pino O; Barbet JP; Chaussain JL
    Pediatrics; 1999 Aug; 104(2 Pt 1):304-8. PubMed ID: 10429013
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?
    Shinawi M; Cain MP; Vanderbrink BA; Grignon DJ; Mensing D; Cooper ML; Bader P; Cheung SW
    Am J Med Genet A; 2010 Jul; 152A(7):1832-7. PubMed ID: 20583182
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. The use of fluorescence in situ hybridization in the diagnosis of hidden mosaicism: apropos of three cases of sex chromosome anomalies.
    Maciel-Guerra AT; Paulo JD; Santos AP; Guaragna-Filho G; Andrade JG; Siviero-Miachon AA; Spinola-Castro AM; Guerra-Júnior G
    Arq Bras Endocrinol Metabol; 2012 Nov; 56(8):545-51. PubMed ID: 23295296
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Detection of the SRY gene in patients with Turner Syndrome.
    Kurnaz E; Çetinkaya S; Savaş-Erdeve Ş; Aycan Z
    J Gynecol Obstet Hum Reprod; 2019 Apr; 48(4):265-267. PubMed ID: 30685428
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A mutation in the 5' non-high mobility group box region of the SRY gene in patients with Turner syndrome and Y mosaicism.
    Canto P; de la Chesnaye E; López M; Cervantes A; Chávez B; Vilchis F; Reyes E; Ulloa-Aguirre A; Kofman-Alfaro S; Méndez JP
    J Clin Endocrinol Metab; 2000 May; 85(5):1908-11. PubMed ID: 10843173
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Characterization of an isodicentric Y-chromosome for the long arm in a newborn with mixed gonadal dysgenesis.
    Kohn B; Kleyman SM; Conte RA; Macera MJ; Glassberg K; Verma RS
    Ann Genet; 1997; 40(1):10-3. PubMed ID: 9150844
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of Y chromosome sequences in a 45,X/46,XXq--patient by Southern blot analysis of PCR-amplified DNA and fluorescent in situ hybridization (FISH).
    Kocova M; Siegel SF; Wenger SL; Lee PA; Nalesnik M; Trucco M
    Am J Med Genet; 1995 Feb; 55(4):483-8. PubMed ID: 7762591
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial gonadal dysgenesis in a patient with a marker Y chromosome.
    Fechner PY; Smith KD; Jabs EW; Migeon CJ; Berkovitz GD
    Am J Med Genet; 1992 Apr; 42(6):807-12. PubMed ID: 1313209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pathogenetics of 45,X/46,XY gonadal mosaicism.
    Reddy KS; Sulcova V
    Cytogenet Cell Genet; 1998; 82(1-2):52-7. PubMed ID: 9763660
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Screening for mutations in the SRY gene in patients with mixed gonadal dysgenesis or with Turner syndrome and Y mosaicism.
    Canto P; Galicia N; Söderlund D; Escudero I; Méndez JP
    Eur J Obstet Gynecol Reprod Biol; 2004 Jul; 115(1):55-8. PubMed ID: 15223166
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 45,X/46,XY mosaicism. A clinical review and report of ten cases.
    Knudtzon J; Aarskog D
    Eur J Pediatr; 1987 May; 146(3):266-71. PubMed ID: 3595646
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of sex chromosome aneuploidy in 41 patients with Turner syndrome: a study of 'hidden' mosaicism.
    Fernández-García R; García-Doval S; Costoya S; Pásaro E
    Clin Genet; 2000 Sep; 58(3):201-8. PubMed ID: 11076042
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.