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Journal Abstract Search

86 related items for PubMed ID: 752070

  • 21. 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; 50(4):291-300. PubMed ID: 17584536
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  • 22. Two cases of Y; autosome translocations: A 45,X male and a clinically trisomy 18 patient.
    Farah SB, Ramos CF, de Mello MP, Sartorato EL, Horelli-Kuitunen N, Lopes VL, Cavalcanti DP, Hackel C.
    Am J Med Genet; 1994 Feb 15; 49(4):388-92. PubMed ID: 8160730
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  • 23. Unique t(Y;1)(q12;q12) reciprocal translocation with loss of the heterochromatic region of chromosome 1 in a male with azoospermia due to meiotic arrest: a case report.
    Pinho MJ, Neves R, Costa P, Ferrás C, Sousa M, Alves C, Almeida C, Fernandes S, Silva J, Ferrás L, Barros A.
    Hum Reprod; 2005 Mar 15; 20(3):689-96. PubMed ID: 15665019
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  • 24. Coincidence of paternal 13pYq translocation and maternal increased 13p NOR activity in a child with arthrogryposis and other malformations.
    Bajnóczky K, Meggyessy V.
    Acta Paediatr Hung; 1985 Mar 15; 26(2):151-6. PubMed ID: 4041282
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  • 25. Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female.
    Page DC, Fisher EM, McGillivray B, Brown LG.
    Nature; 1990 Jul 19; 346(6281):279-81. PubMed ID: 1973823
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  • 26. Case of (Y;1) familial translocation.
    Teyssier M, Rafat A, Pugeat M.
    Am J Med Genet; 1993 May 15; 46(3):339-40. PubMed ID: 8488881
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  • 27. Ambiguous genitalia and mental retardation associated with a translocation 46, XX, t(9; 10) and a deletion in 9q.
    Jenkins EC, Chaganti RS, Wilbur L, German J.
    Birth Defects Orig Artic Ser; 1976 May 15; 12(5):169-73. PubMed ID: 953219
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  • 29. Prenatal detection of a de novo Yqh-acrocentric translocation.
    Ng LK, Kwok YK, Tang LY, Ng PP, Ghosh A, Lau ET, Tang MH.
    Clin Biochem; 2006 Mar 15; 39(3):219-23. PubMed ID: 16515778
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  • 30. Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
    Iourov IY, Vorsanova SG, Liehr T, Monakhov VV, Soloviev IV, Yurov YB.
    Cytogenet Genome Res; 2008 Mar 15; 121(3-4):302-6. PubMed ID: 18758177
    [Abstract] [Full Text] [Related]

  • 31. Characterization of a de novo t(Y;9) (q11.2;q22) by FISH technique.
    Conte RA, Kleyman SM, Klein V, Bialer MG, Verma RS.
    Ann Genet; 1996 Mar 15; 39(1):10-5. PubMed ID: 9297438
    [Abstract] [Full Text] [Related]

  • 32. Klinefelter variant mosaic with a reciprocal translocation t(1;7).
    Vasu V, Chandra N, Jayashankar M, Santhiya ST.
    Fertil Steril; 2008 Nov 15; 90(5):2017.e15-7. PubMed ID: 18304545
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  • 36. Mosaic 46, XY/47,XY, + der(18)t(Y;18)(q11.22;q11.2) karyotype, moderate mental retardation and non-specific dysmorphism.
    Fryns JP, Kleczkowska A, Van Den Berghe H.
    Genet Couns; 1990 Nov 15; 1(2):173-7. PubMed ID: 2081001
    [No Abstract] [Full Text] [Related]

  • 37. [Translocation t(Y;14) in an azoospermic man].
    Laurent C, Dutrillaux B.
    Ann Genet; 1976 Sep 15; 19(3):207-9. PubMed ID: 1086631
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  • 38. A new family with a satellited Y.
    Shabtai F, Eilam N, Elian E, Halbrecht I.
    Ann Genet; 1981 Sep 15; 24(4):223-5. PubMed ID: 6977302
    [No Abstract] [Full Text] [Related]

  • 39. A case of a reciprocal translocation between the Y and no. 1 chromosomes.
    Narahara K, Yabuuchi H, Kimura S, Kimoto H.
    Jinrui Idengaku Zasshi; 1978 Sep 15; 23(3):225-31. PubMed ID: 732018
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  • 40. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
    Qumsiyeh MB, Dalton JD, Gordon PL, Wilroy RS, Tharapel AT.
    Am J Med Genet; 1992 Jan 01; 42(1):109-11. PubMed ID: 1308348
    [Abstract] [Full Text] [Related]

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