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176 related items for PubMed ID: 11330396

  • 1. 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; 9(3):215-22. PubMed ID: 11330396
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. Satellited Y chromosomes: structure, origin, and clinical significance.
    Schmid M, Haaf T, Solleder E, Schempp W, Leipoldt M, Heilbronner H.
    Hum Genet; 1984 May; 67(1):72-85. PubMed ID: 6745929
    [Abstract] [Full Text] [Related]

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

  • 5. 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]

  • 6. [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(2):86-90. PubMed ID: 6604491
    [Abstract] [Full Text] [Related]

  • 7. 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; 96(5):585-8. PubMed ID: 8530007
    [Abstract] [Full Text] [Related]

  • 8. A family case of fertile human 45,X,psu dic(15;Y) males.
    Wimmer R, Schempp W, Gopinath PM, Nagarajappa CS, Chandra N, Palaniappan I, Hansmann I.
    Cytogenet Genome Res; 2006 Nov; 115(1):94-8. PubMed ID: 16974089
    [Abstract] [Full Text] [Related]

  • 9. 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]

  • 10. Complex distal 10q rearrangement in a girl with mild intellectual disability: follow up of the patient and review of the literature of non-acrocentric satellited chromosomes.
    Sarri C, Douzgou S, Gyftodimou Y, Tümer Z, Ravn K, Pasparaki A, Sarafidou T, Kontos H, Kokotas H, Karadima G, Grigoriadou M, Pandelia E, Theodorou V, Moschonas NK, Petersen MB.
    Am J Med Genet A; 2011 Nov; 155A(11):2841-54. PubMed ID: 21964744
    [Abstract] [Full Text] [Related]

  • 11. Origin and structure of a satellited Y chromosome.
    Martin Lucas MA, Pérez Castillo A, Abrisqueta JA.
    Ann Genet; 1984 Nov; 27(3):184-6. PubMed ID: 6334485
    [Abstract] [Full Text] [Related]

  • 12. Pseudoautosomal abnormalities in terminal AZFb+c deletions are associated with isochromosomes Yp and may lead to abnormal growth and neuropsychiatric function.
    Castro A, Rodríguez F, Flórez M, López P, Curotto B, Martínez D, Maturana A, Lardone MC, Palma C, Mericq V, Ebensperger M, Cassorla F.
    Hum Reprod; 2017 Feb; 32(2):465-475. PubMed ID: 28057878
    [Abstract] [Full Text] [Related]

  • 13. Molecular cytogenetic study of short arm aberrations in human D, G group chromosomes.
    Wang Y, Cheng Z, Gao C, Fu S, Wang S, Fu H, Ye L, Ma S.
    Chin Med Sci J; 1992 Mar; 7(1):27-31. PubMed ID: 1421359
    [Abstract] [Full Text] [Related]

  • 14. [Remarks on a satellited Y chromosome (author's transl)].
    Genest P.
    Sem Hop; 1992 Mar; 55(15-16):799-800. PubMed ID: 227075
    [Abstract] [Full Text] [Related]

  • 15. Characterization of a (Y;4) translocation by DNA hybridization.
    Andersson M, Page DC, Brown LG, Elfving K, de la Chapelle A.
    Hum Genet; 1988 Apr; 78(4):377-81. PubMed ID: 3360449
    [Abstract] [Full Text] [Related]

  • 16. A molecular deletion map of the Y chromosome long arm defining X and autosomal homologous regions and the localisation of the HYA locus to the proximal region of the Yq euchromatin.
    O'Reilly AJ, Affara NA, Simpson E, Chandler P, Goulmy E, Ferguson-Smith MA.
    Hum Mol Genet; 1992 Sep; 1(6):379-85. PubMed ID: 1301911
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. 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]

  • 19. [A satellited Y chromosome].
    Genest P.
    Ann Genet; 1978 Dec; 21(4):237-8. PubMed ID: 314263
    [Abstract] [Full Text] [Related]

  • 20. Detection of t(X;Y) in 2 XX males using fluorescent in situ hybridization.
    Taiar N, Qumsiyeh MB, Croteau S, Rollet J, Benkhalifa M.
    Ann Genet; 1995 Dec; 38(2):102-5. PubMed ID: 7486824
    [Abstract] [Full Text] [Related]

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