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 *

88 related articles for article (PubMed ID: 2565452)

  • 1. Prenatally diagnosed 45,X/46,XY and normal phenotype.
    Chang HJ; Clark RD; Bachman H
    Lancet; 1989 Apr; 1(8644):961-2. PubMed ID: 2565452
    [No Abstract]   [Full Text] [Related]  

  • 2. Prenatal diagnosis of 45, X/46, XY.
    Waurin JL; Adams JE; Baramki TA
    Md Med J; 1985 Sep; 34(9):883-4. PubMed ID: 3851135
    [No Abstract]   [Full Text] [Related]  

  • 3. 45,X/46,XY mosaicism: the role of ultrasound in prenatal diagnosis and counselling.
    Lazebnik N; Filkins KA; Jackson CL; Linn KB; Doshi NN; Hogge WA
    Ultrasound Obstet Gynecol; 1996 Nov; 8(5):325-8. PubMed ID: 8978006
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The phenotype of 45,X/46,XY mosaicism: an analysis of 92 prenatally diagnosed cases.
    Chang HJ; Clark RD; Bachman H
    Am J Hum Genet; 1990 Jan; 46(1):156-67. PubMed ID: 2294747
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Diagnostic applications of H-Y serology: H-Y negative phenotype in cells from 45,X/46,XY fetus with testes.
    Lieber E; Wachtel SS; Aftalion B; Zaslav AL
    Clin Genet; 1986 Nov; 30(5):366-73. PubMed ID: 3802555
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 45,X/46,XY mosaicism: contrast of prenatal and postnatal diagnosis.
    Wheeler M; Peakman D; Robinson A; Henry G
    Am J Med Genet; 1988 Mar; 29(3):565-71. PubMed ID: 3376999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Antenatal diagnosis of 45,X/48,XYYY.
    Bryke CR; Mahoney MJ; Yang-Feng TL
    Am J Med Genet; 1989 Oct; 34(2):207-10. PubMed ID: 2816999
    [TBL] [Abstract][Full Text] [Related]  

  • 9. XX/XY chimerism encountered during prenatal diagnosis.
    Freiberg AS; Blumberg B; Lawce H; Mann J
    Prenat Diagn; 1988 Jul; 8(6):423-6. PubMed ID: 3211844
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic hygroma and 45,X/46,XY mosaicism.
    Verp MS; Sheikh Z; Amarose AP; Cibils LA
    Am J Med Genet; 1989 Jul; 33(3):402-4. PubMed ID: 2679092
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Confirmation of prenatal diagnosis of sex chromosome mosaicism.
    McFadden DE; Kalousek DK
    Am J Med Genet; 1989 Apr; 32(4):495-7. PubMed ID: 2773991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of 45,X/46,XX mosaicism and 45,X: implications for postnatal outcome.
    Koeberl DD; McGillivray B; Sybert VP
    Am J Hum Genet; 1995 Sep; 57(3):661-6. PubMed ID: 7668295
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 45,X/46,XX/47,XXX phenotype.
    Lebel RR; Elejalde BR; de Elejalde MM; Avila T
    Prenat Diagn; 1993 Dec; 13(12):1165-6. PubMed ID: 8177840
    [No Abstract]   [Full Text] [Related]  

  • 14. Prenatal diagnosis of 45,X/46,XY mosaicism--a review and update.
    Hsu LY
    Prenat Diagn; 1989 Jan; 9(1):31-48. PubMed ID: 2664755
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Prenatal diagnosis of a 46,XX,inv(12)pat/47,XX,i(Xq),inv(12)pat.
    Varela M; Wang N; Cerrillo M
    Hum Genet; 1987 Jan; 75(1):93-4. PubMed ID: 3804337
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Antenatal detection of a 46,XY/47,XYY mosaicism (author's transl)].
    Mancinelli S; Loreto Peña M; Vivaldi E; Stuardo MC
    Rev Med Chil; 1979 Apr; 107(4):324-7. PubMed ID: 504838
    [No Abstract]   [Full Text] [Related]  

  • 18. Down's/Turner's mosaicism. Double aneuploidy as a rare cause of missed prenatal diagnosis of chromosomal abnormality.
    MacFaul R; Turner T; Mason MK
    Arch Dis Child; 1981 Dec; 56(12):962-3. PubMed ID: 6460476
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probe.
    Disteche C; Luthy D; Haslam DB; Hoar D
    Hum Genet; 1984; 67(2):222-4. PubMed ID: 6745944
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Natural history of prenatally diagnosed 46,X,isodicentric Y.
    Willis MJ; Bird LM; Dell'aquilla M; Jones MC
    Prenat Diagn; 2006 Feb; 26(2):134-7. PubMed ID: 16463293
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.