BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 569516)

  • 1. Cytogenetic and clinical notes on a girl with a 46,X,i(Yq) karyotype, H-Y antigen-negative, and a gonadoblastoma.
    Rary JM; Cummings DK; Jones HW; Rock JA; Julian CG
    Birth Defects Orig Artic Ser; 1978; 14(6C):97-107. PubMed ID: 569516
    [No Abstract]   [Full Text] [Related]  

  • 2. Bilateral gonadoblastoma in a phenotypic female with 45,X/46,X, dicentric iso Y [45,X/46,X,idic(Yq)] mosaicism.
    King CR; Cook DM
    Birth Defects Orig Artic Ser; 1978; 14(6C):109-22. PubMed ID: 569512
    [No Abstract]   [Full Text] [Related]  

  • 3. The Turner syndrome and the Y chromosome: mechanisms of diminished Y-determined maleness.
    Riccardi VM; Duck S; Katayama P
    Birth Defects Orig Artic Ser; 1978; 14(6C):123-32. PubMed ID: 569513
    [No Abstract]   [Full Text] [Related]  

  • 4. H-Y gene expression in apparent absence of the long arm of the Y chromosome.
    Moreira-Filho CA; Otto PG; Frota-Pessoa O
    Am J Med Genet; 1979; 4(2):135-9. PubMed ID: 117709
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Assignment of the H-Y antigen gene to the short arm of chromosome Y.
    Rary JM; Cummings DK; Jones HW; Rock JA
    J Hered; 1979; 70(1):78-80. PubMed ID: 469228
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies.
    Patil SR; Kaiser-McCaw B; Hecht F; Linder D; Lovrien EW
    Birth Defects Orig Artic Ser; 1978; 14(6B):297-301. PubMed ID: 728570
    [No Abstract]   [Full Text] [Related]  

  • 7. Gonadoblastoma in Turner syndrome patients with nonmosaic 45,X karyotype and Y chromosome sequences.
    Canto P; Kofman-Alfaro S; Jiménez AL; Söderlund D; Barrón C; Reyes E; Méndez JP; Zenteno JC
    Cancer Genet Cytogenet; 2004 Apr; 150(1):70-2. PubMed ID: 15041227
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Phenotype/karyotype correlations of Y chromosome aneuploidy with emphasis on structural aberrations in postnatally diagnosed cases.
    Hsu LY
    Am J Med Genet; 1994 Nov; 53(2):108-40. PubMed ID: 7856637
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case with mosaic di-, tetra-, and octacentric ring Y chromosomes.
    Henegariu O; Pescovitz OH; Vance GH; Verbrugge J; Heerema NA
    Am J Med Genet; 1997 Sep; 71(4):426-9. PubMed ID: 9286449
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Combined cytogenetic techniques and non-fluorescent Y. Cytologic evidences of dic(Yp)(q11) in a previously interpreted 46,X,Yq-.
    de Almeida JC; Llerena JC; Jung M; Martins RR; Gomes DM; Reis DF; Cunha AG
    Ann Genet; 1986; 29(2):114-8. PubMed ID: 3490206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Identification of sex chromosome markers using fluorescence in situ hybridization (FISH)].
    González-del-Angel A; Blanco B; del Castillo V; Carnevale A
    Rev Invest Clin; 1995; 47(2):117-25. PubMed ID: 7610280
    [TBL] [Abstract][Full Text] [Related]  

  • 13. H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesis.
    Haseltine FP; Lynch VA; Van Dyke DL; Breg WR; Francke U
    Am J Med Genet; 1982 Oct; 13(2):115-23. PubMed ID: 7137226
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Structural abnormalities of the Y chromosome. Observations in ten cases].
    Mattei JF; Mattei MG; Lucas C; Giraud F
    J Genet Hum; 1979 Mar; 27(1):53-66. PubMed ID: 479854
    [TBL] [Abstract][Full Text] [Related]  

  • 15. H-Y typing by ELISA in a 46,X,dic(Y)(q11.2101) male: effects of a nonmosaic Yp duplication.
    Moreira-Filho CA; Wachtel SS; Daniel A; Priest JH
    Am J Med Genet; 1987 Mar; 26(3):709-17. PubMed ID: 3565484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dicentric Y chromosome in a patient with gonadal dysgenesis and seminoma.
    Ponzio G; DeMarchi M; Carbonara A; Godano A; Massara F
    Hum Genet; 1981; 58(3):282-4. PubMed ID: 7327549
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosome.
    Savary JB; Vasseur F; Flactif M; Willatt L; Lefebvre J; Ferguson-Smith MA; Deminatti MM
    Ann Genet; 1992; 35(3):134-9. PubMed ID: 1466561
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Presence of Y chromosome sequences and their effect on the phenotype of six patients with Y chromosome anomalies.
    Shankman S; Spurdle AB; Morris D; Rosendorff J; Marques I; Bernstein R; Ramsay M
    Am J Med Genet; 1995 Jan; 55(3):269-75. PubMed ID: 7726221
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Gonadoblastoma in a patient with an isodicentric X chromosome.
    Katayama KP; Roesler MR; Dungar CF; Mattingly RF
    Clin Genet; 1983 Nov; 24(5):355-8. PubMed ID: 6652946
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic analysis of ependymoma and teratoma of the ovary.
    Yang-Feng TL; Katz SN; Cacangiu ML; Schwartz PE
    Cancer Genet Cytogenet; 1988 Oct; 35(1):83-9. PubMed ID: 3180015
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.