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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

146 related items for PubMed ID: 9350813

  • 1. Characterisation of a satellited non-fluorescent Y chromosome (Y[nfqs]) by FISH.
    Verma RS, Gogineni SK, Kleyman SM, Conte RA.
    J Med Genet; 1997 Oct; 34(10):817-8. PubMed ID: 9350813
    [Abstract] [Full Text] [Related]

  • 2. 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; 9(3):215-22. PubMed ID: 11330396
    [Abstract] [Full Text] [Related]

  • 3. Molecular cytogenetic characterization of three familial cases of satellited Y chromosomes.
    Wilkinson TA, Crolla JA.
    Hum Genet; 1993 May; 91(4):389-91. PubMed ID: 8500794
    [Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. Coexistence of inverted Y, chromosome 15p+ and abnormal phenotype.
    Acar H, Cora T, Erkul I.
    Genet Couns; 1999 Jun; 10(2):163-70. PubMed ID: 10422010
    [Abstract] [Full Text] [Related]

  • 6. Molecular characterization of an unusual variant of the short arm of chromosome 15 by FISH-technique.
    Verma RS, Kleyman SM, Conte RA.
    Jpn J Hum Genet; 1996 Sep; 41(3):307-11. PubMed ID: 8996966
    [Abstract] [Full Text] [Related]

  • 7. A case of prenatal diagnosis of a familial satellited Yq chromosome.
    Tsita KP, Vallas OS, Velissariou PJ, Lyberatou-Moraitou EK.
    Clin Genet; 1989 Jan; 35(1):70-4. PubMed ID: 2924432
    [Abstract] [Full Text] [Related]

  • 8. Deleted Yq in the sterile son of a man with a satellited Y chromosome (Yqs).
    Chandley AC, Gosden JR, Hargreave TB, Spowart G, Speed RM, McBeath S.
    J Med Genet; 1989 Mar; 26(3):145-53. PubMed ID: 2709392
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. A DA/DAPI positive human 14p heteromorphism defined by fluorescence in-situ hybridisation using chromosome 15-specific probes D15Z1 (satellite III) and p-TRA-25 (alphoid).
    Stergianou K, Gould CP, Waters JJ, Hultén MA.
    Hereditas; 1993 May; 119(2):105-10. PubMed ID: 8106258
    [Abstract] [Full Text] [Related]

  • 11. Two cases of prenatal diagnosis of a satellited Yq chromosome.
    Bayless-Underwood L, Cho S, Ward B, Robinson A.
    Clin Genet; 1983 Nov; 24(5):359-64. PubMed ID: 6686092
    [Abstract] [Full Text] [Related]

  • 12. 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 Nov; 50(4):291-300. PubMed ID: 17584536
    [Abstract] [Full Text] [Related]

  • 13. Clinical management of a rare de novo translocation 46,X,t(Y;15) (p11.2 approximately 11.3;q11.2).ish t(Y;15)(DYZ3+,AMELY+,SNRPN+;D15Z+) found prenatally.
    Reddy KS.
    Prenat Diagn; 1998 Mar; 18(3):294-7. PubMed ID: 9556048
    [Abstract] [Full Text] [Related]

  • 14. Reassessment of presumed Y/22 and Y/15 translocations in man using a new technique.
    Spowart G.
    Cytogenet Cell Genet; 1979 Mar; 23(1-2):90-4. PubMed ID: 83932
    [Abstract] [Full Text] [Related]

  • 15. Comparative analysis of Y chromosome structure in Bos taurus and B. indicus by FISH using region-specific, microdissected, and locus-specific DNA probes.
    Goldammer T, Brunner RM, Schwerin M.
    Cytogenet Cell Genet; 1997 Mar; 77(3-4):238-41. PubMed ID: 9284924
    [Abstract] [Full Text] [Related]

  • 16. Role of multicolor fluorescence in situ hybridization (FISH) in simultaneous detection of probe sets for chromosome 18, X and Y in uncultured amniotic fluid cells.
    Kim JI, Rhee JH.
    J Korean Med Sci; 1999 Aug; 14(4):438-42. PubMed ID: 10485625
    [Abstract] [Full Text] [Related]

  • 17. Different phenotypes in two cases of an apparently identical familial (Yq;13p) translocation.
    Doneda L, Magnani I, Tibiletti MG, Dalprà L, Larizza L.
    Hum Reprod; 1992 Apr; 7(4):495-9. PubMed ID: 1522192
    [Abstract] [Full Text] [Related]

  • 18. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
    Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.
    Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
    [Abstract] [Full Text] [Related]

  • 19. AZFc deletion detected in a newborn with prenatally diagnosed Yq deletion.
    Tóth A, Tardy EP, Gombos S, Hajdu K, Bátorfi J, Krausz C.
    Prenat Diagn; 2001 Apr; 21(4):253-5. PubMed ID: 11288112
    [Abstract] [Full Text] [Related]

  • 20. Molecular characterization of a Y;15 translocation segregating in a family.
    Alitalo T, Tiihonen J, Hakola P, de la Chapelle A.
    Hum Genet; 1988 May; 79(1):29-35. PubMed ID: 3366460
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 8.