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Journal Abstract Search

136 related items for PubMed ID: 9093147

  • 1. Evaluation of satellited Y chromosome (Yqs) detected during prenatal diagnosis.
    Haddad BR, Huang Y, Wyandt H, Milunsky A.
    Acta Obstet Gynecol Scand; 1997 Mar; 76(3):281-3. PubMed ID: 9093147
    [No Abstract] [Full Text] [Related]

  • 2. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
    Chen CP, Devriendt K, Chern SR, Lee CC, Wang W, Lin SP.
    Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
    Velissariou V, Antoniadi T, Patsalis P, Christopoulou S, Hatzipouliou A, Donoghue J, Bakou K, Kaminopetros P, Athanassiou V, Petersen MB.
    Prenat Diagn; 2001 Jun; 21(6):484-7. PubMed ID: 11438955
    [Abstract] [Full Text] [Related]

  • 4. [Preimplantation genetic diagnosis using the FISH technic].
    Plachot M.
    Contracept Fertil Sex; 1999 Jun; 27(7-8):491-4. PubMed ID: 10495565
    [No Abstract] [Full Text] [Related]

  • 5. [Prenatal diagnosis of a translocation (X;Y) and genetic counseling].
    Stora-de Novion H, Petit C, Raynaud S, Ayraud N.
    J Genet Hum; 1989 Sep; 37(3):263-7. PubMed ID: 2625630
    [Abstract] [Full Text] [Related]

  • 6. The usefulness of NOR and RFA banding in prenatal diagnosis: a case report.
    Sciorra LJ, Rajendra B, Cummings E, Ekblom L, Lee M.
    Am J Med Genet; 1981 Sep; 10(2):147-9. PubMed ID: 7315871
    [Abstract] [Full Text] [Related]

  • 7. Loss of the Y chromosome PAR2 region and additional rearrangements in two familial cases of satellited Y chromosomes: cytogenetic and molecular analysis.
    Velissariou V, Sismani C, Christopoulou S, Kaminopetros P, Hatzaki A, Evangelidou P, Koumbaris G, Bartsocas CS, Stylianidou G, Skordis N, Diakoumakos A, Patsalis PC.
    Eur J Med Genet; 2007 Sep; 50(4):291-300. PubMed ID: 17584536
    [Abstract] [Full Text] [Related]

  • 8. [Fluorescent in situ hybridization (FISH). A new dimension of genetics].
    Blennow ES.
    Lakartidningen; 1994 Oct 26; 91(43):3901-5. PubMed ID: 7967959
    [No Abstract] [Full Text] [Related]

  • 9. [Unusual chromosomal rearrangement. An autosomal telomeric translocation on a multicentury satellited Y (Yqs) chromosome].
    Genest P, Genest FB, Gagnon-Blais D.
    Ann Genet; 1983 Oct 26; 26(2):86-90. PubMed ID: 6604491
    [Abstract] [Full Text] [Related]

  • 10. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells].
    Marguerat P, Gaide AC, Thonney F, Schorderet D.
    Rev Med Suisse Romande; 2000 May 26; 120(5):401-7. PubMed ID: 10911743
    [Abstract] [Full Text] [Related]

  • 11. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
    Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A.
    Prenat Diagn; 2007 Nov 26; 27(11):1064-6. PubMed ID: 17654752
    [No Abstract] [Full Text] [Related]

  • 12. Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p.
    De Pater JM, Van Tintelen JP, Stigter R, Brouwers HA, Scheres JM.
    Genet Couns; 2000 Nov 26; 11(3):241-7. PubMed ID: 11043432
    [Abstract] [Full Text] [Related]

  • 13. Detection of translocations involving the Y-chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH.
    Verlinsky Y, Ginsberg N, Chmura M, White M, Strom C, Kuliev A.
    Prenat Diagn; 1998 Apr 26; 18(4):390-2. PubMed ID: 9602488
    [Abstract] [Full Text] [Related]

  • 14. Rapid prenatal diagnosis of chromosome abnormalities.
    Tan SY, Chan WB, Cheng WC, Hagarty A, Lim KT, Quaife R.
    Singapore Med J; 2000 Oct 26; 41(10):493-7. PubMed ID: 11281441
    [Abstract] [Full Text] [Related]

  • 15. Loss of the Y chromosomal PAR2-region in four familial cases of satellited Y chromosomes (Yqs).
    Kühl H, Röttger S, Heilbronner H, Enders H, Schempp W.
    Chromosome Res; 2001 Oct 26; 9(3):215-22. PubMed ID: 11330396
    [Abstract] [Full Text] [Related]

  • 16. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L, Li H, Xue YQ, Pan JL, Wu YF, Lu M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec 26; 21(6):611-4. PubMed ID: 15583994
    [Abstract] [Full Text] [Related]

  • 17. A de novo satellited short arm of the Y chromosome possibly resulting from an unstable translocation.
    Lin CL, Gibson L, Pober B, Yang-Feng TL.
    Hum Genet; 1995 Nov 26; 96(5):585-8. PubMed ID: 8530007
    [Abstract] [Full Text] [Related]

  • 18. Report of a family case of satellited Y chromosome associated with a severe oligoasthenoteratospermia. A review of the literature.
    Couturier-Turpin MH, Ingster O, Salat-Baroux J, Feldmann G.
    Ann Genet; 1994 Nov 26; 37(4):200-6. PubMed ID: 7710256
    [Abstract] [Full Text] [Related]

  • 19. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
    Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.
    Ann Genet; 1998 Nov 26; 41(3):133-40. PubMed ID: 9833066
    [Abstract] [Full Text] [Related]

  • 20. [Prenatal diagnosis from a human genetic viewpoint today and tomorrow].
    Schwinger E, Schürmann M.
    Gynakologe; 1984 Mar 26; 17(1):13-8. PubMed ID: 6724336
    [No Abstract] [Full Text] [Related]

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