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Journal Abstract Search

151 related items for PubMed ID: 2665261

  • 41. A 45,X sterile male with Yp disguised as 21p.
    Dávalos IP, Rivera H, Vásquez AI, Gutiérrez-Angulo M, Hernández-Vázquez MC, Cortina-Luna FA, Wong-Ley LE, Domínguez-Quezada MG.
    Am J Med Genet; 2002 Aug 01; 111(2):202-4. PubMed ID: 12210351
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  • 42. Y;autosome translocations and mosaicism in the aetiology of 45,X maleness: assignment of fertility factor to distal Yq11.
    Andersson M, Page DC, Pettay D, Subrt I, Turleau C, de Grouchy J, de la Chapelle A.
    Hum Genet; 1988 May 01; 79(1):2-7. PubMed ID: 3163319
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  • 45. A dysmorphic newborn with 45,X,der(1)inv(1)(p13;qter)t(Y;1)(pter-->q11;p13),-Y de novo karyotype.
    Tatar A, Oztas S, Yakut T, Ors R.
    Genet Couns; 2005 May 01; 16(2):173-7. PubMed ID: 16080298
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  • 49. A case of azoospermia in a bull carrying a Y-autosome reciprocal translocation.
    Iannuzzi L, Molteni L, Di Meo GP, De Giovanni A, Perucatti A, Succi G, Incarnato D, Eggen A, Cribiu EP.
    Cytogenet Cell Genet; 2001 May 01; 95(3-4):225-7. PubMed ID: 12063403
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  • 51. A Rare 46,X,t(Y;10)(q12;p14) Balanced Translocation in Non-Obstructive Azoospermic Patient with Elevated FSH and LH Levels.
    Jahan Syeeda Khursheed K, Rahman Kaleemullah M, Joseph A, Hasan Al Durazi M, Bakhiet M.
    Case Rep Genet; 2023 May 01; 2023():6722623. PubMed ID: 38025941
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  • 53. Fluorescene in situ hybridization establishes homology between human and silvered leaf monkey chromosomes, reveals reciprocal translocations between chromosomes homologous to human Y/5, 1/9, and 6/16, and delineates an X1X2Y1Y2/X1X1X2X2 sex-chromosome system.
    Bigoni F, Koehler U, Stanyon R, Ishida T, Wienberg J.
    Am J Phys Anthropol; 1997 Mar 01; 102(3):315-27. PubMed ID: 9098501
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  • 54. Reproductive outcome of a case with familial balanced translocation t(3;6): implications for genetic counseling.
    Zhang HG, Liu XY, Hou Y, Chen S, Deng S, Liu RZ.
    Genet Mol Res; 2015 Mar 31; 14(1):2809-15. PubMed ID: 25867430
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  • 55. 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 Mar 31; 38(2):102-5. PubMed ID: 7486824
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  • 56. A familial extra small marker autosome in persons with normal phenotype.
    Fried K, Rosenblatt M.
    Hum Hered; 1979 Mar 31; 29(6):371-3. PubMed ID: 511193
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  • 59. X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.
    Madan K, Hompes PG, Schoemaker J, Ford CE.
    Hum Genet; 1981 Mar 31; 59(4):290-6. PubMed ID: 7333583
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  • 60. Cytogenetic and Y chromosome microdeletion screening studies in infertile males with Oligozoospermia and Azoospermia in Southeast Turkey.
    Balkan M, Tekes S, Gedik A.
    J Assist Reprod Genet; 2008 Mar 31; 25(11-12):559-65. PubMed ID: 18953646
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