BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

130 related articles for article (PubMed ID: 565337)

  • 1. Centromere inactivation in a case of Turner variant with two dicentric iso-long arm Y chromosomes.
    Schmid W; D'Apuzzo V
    Hum Genet; 1978 Mar; 41(2):217-23. PubMed ID: 565337
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two dicentric Y isochromosomes, one without and the Yqh heterochromatic segment: review of the Y isochromosomes.
    Daniel A; Lyons N; Casey JH; Gras L
    Hum Genet; 1980; 54(1):31-9. PubMed ID: 7190126
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Dicentric Yp chromosome as one of the reasons for the absence of fluorescence in human Y chromosome].
    Verlinskaia DK; Prozorova MV
    Tsitologiia; 1983 Jun; 25(6):696-8. PubMed ID: 6684338
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An investigation of ring and dicentric chromosomes found in three Turner's syndrome patients using DNA analysis and in situ hybridisation with X and Y chromosome specific probes.
    Cooper C; Crolla JA; Laister C; Johnston DI; Cooke P
    J Med Genet; 1991 Jan; 28(1):6-9. PubMed ID: 1999837
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. A dicentric Y chromosome without evidence of sex chromosomal mosaicism, 46,XYqdic, in a patient with features of Turner's syndrome.
    Armendares S; Buentello L; Salamanca F; Cantu-Garza JM
    J Med Genet; 1972 Mar; 9(1):96-100. PubMed ID: 5063516
    [No Abstract]   [Full Text] [Related]  

  • 7. Dicentric X isochromosomes in man.
    Howell RT; Roberts SH; Beard RJ
    J Med Genet; 1976 Dec; 13(6):496-500. PubMed ID: 1018308
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A tdic(5;15)(p31;p11) chromosome showing variation for constriction in the centromeric regions in a patient with the cri du chat syndrome.
    Dewald GW; Boros SJ; Conroy MM; Dahl RJ; Spurbeck JL; Vitek HA
    Cytogenet Cell Genet; 1979; 24(1):15-26. PubMed ID: 456039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nonfluorescent Y chromosomes. Cytologic evidence of origin.
    Magenis E; Donlon T
    Hum Genet; 1982; 60(2):133-8. PubMed ID: 7076253
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Detection of Y-chromosomal DNA with marker chromosomes in Turner's syndrome.
    Kuo PL; Wu RC; Tzeng CC; Lin SJ; Liu SS; Huang KE
    J Formos Med Assoc; 1995 Aug; 94(8):474-80. PubMed ID: 7549576
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Symptoms of Turner's syndrome and interstitial heterochromatin in i(Xq).
    Yanagisawa S; Yokoyama H
    Clin Genet; 1975 Apr; 7(4):299-303. PubMed ID: 47795
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [X isochromosomes: delayed diagnosis of Turner's syndrome].
    Cuesta Hernández M; Rueda Valencia ME; Pérez Rodríguez O; López de Lara D
    An Pediatr (Barc); 2015 Jan; 82(1):e131-4. PubMed ID: 25475905
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Localisation of male determining factors in man: a thorough review of structural anomalies of the Y chromosome.
    Davis RM
    J Med Genet; 1981 Jun; 18(3):161-95. PubMed ID: 7017147
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interstitial deletions of repetitive DNA blocks in dicentric human Y chromosomes.
    Köhler MR; Vogt PH
    Chromosoma; 1994 Sep; 103(5):324-30. PubMed ID: 7821087
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dicentric Y chromosome and mixed dysgenesis.
    Weckworth PF; Johnson HW; Pantzar JT; Coleman GU; Masterson JS; McGillivray B; Tze WJ
    J Urol; 1988 Jan; 139(1):91-4. PubMed ID: 2891862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Iso-X chromosomes in primary amenorrhoea and Turner's syndrome - presentation by C-banding (author's transl)].
    Zernahle K
    Zentralbl Gynakol; 1980; 102(3):151-60. PubMed ID: 7211028
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Sex chromosome aberrations in patients with menstruation disorders].
    Midro AT; Panasiuk B; Radwan J; Sipowicz I; Jaworowska B; Korsak E
    J Gynecol Obstet Biol Reprod (Paris); 1990; 19(7):811-6. PubMed ID: 2277162
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Centromere inactivation on a neo-Y fusion chromosome in threespine stickleback fish.
    Cech JN; Peichel CL
    Chromosome Res; 2016 Dec; 24(4):437-450. PubMed ID: 27553478
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dicentric Y chromosome arising via tandem translocation.
    Herva R; Saarinen I; Savikurki H; de la Chapelle A
    Am J Med Genet; 1980; 7(2):115-22. PubMed ID: 7193412
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.