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Journal Abstract Search

383 related items for PubMed ID: 20345472

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  • 2. Molecular genetic and cytogenetic characterization of a partial Xp duplication and Xq deletion in a patient with premature ovarian failure.
    Kim MK, Seok HH, Kim YS, Chin MU, Sung SR, Lee WS, Shim SH, Yoon TK.
    Gene; 2014 Jan 15; 534(1):54-9. PubMed ID: 24148559
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  • 4. Cytogenetic analysis of 531 Chinese women with premature ovarian failure.
    Jiao X, Qin C, Li J, Qin Y, Gao X, Zhang B, Zhen X, Feng Y, Simpson JL, Chen ZJ.
    Hum Reprod; 2012 Jul 15; 27(7):2201-7. PubMed ID: 22513983
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  • 5. Cytogenetics of premature ovarian failure: an investigation on 269 affected women.
    Baronchelli S, Conconi D, Panzeri E, Bentivegna A, Redaelli S, Lissoni S, Saccheri F, Villa N, Crosti F, Sala E, Martinoli E, Volontè M, Marozzi A, Dalprà L.
    J Biomed Biotechnol; 2011 Jul 15; 2011():370195. PubMed ID: 21318170
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  • 6. [Analysis of X chromosome mosaicism in patients with premature ovarian failure by fluorescent in-situ hybridization].
    Diao FY, Xu M, Liu JY.
    Zhonghua Fu Chan Ke Za Zhi; 2003 Jan 15; 38(1):20-3. PubMed ID: 12757653
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  • 7. Cytogenetic abnormalities in Tunisian women with premature ovarian failure.
    Ayed W, Amouri A, Hammami W, Kilani O, Turki Z, Harzallah F, Bouayed-Abdelmoula N, Chemkhi I, Zhioua F, Slama CB.
    C R Biol; 2014 Dec 15; 337(12):691-4. PubMed ID: 25433561
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  • 8. Low-level X chromosome mosaicism in women with sporadic premature ovarian failure.
    Gersak K, Veble A.
    Reprod Biomed Online; 2011 Apr 15; 22(4):399-403. PubMed ID: 21334258
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  • 9. Molecular cytogenetic studies of Xq critical regions in premature ovarian failure patients.
    Portnoï MF, Aboura A, Tachdjian G, Bouchard P, Dewailly D, Bourcigaux N, Frydman R, Reyss AC, Brisset S, Christin-Maitre S.
    Hum Reprod; 2006 Sep 15; 21(9):2329-34. PubMed ID: 16751643
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  • 10. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY, Soloviev IV, Vorsanova SG, Monakhov VV, Yurov YB.
    J Histochem Cytochem; 2005 Mar 15; 53(3):401-8. PubMed ID: 15750029
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  • 15. Multiple myeloma: high incidence of chromosomal aneuploidy as detected by interphase fluorescence in situ hybridization.
    Drach J, Schuster J, Nowotny H, Angerler J, Rosenthal F, Fiegl M, Rothermundt C, Gsur A, Jäger U, Heinz R.
    Cancer Res; 1995 Sep 01; 55(17):3854-9. PubMed ID: 7641204
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  • 17. Cryptic Xp duplication including the SHOX gene in a woman with 46,X, del(X)(q21.31) and premature ovarian failure.
    Tachdjian G, Aboura A, Portnoï MF, Pasquier M, Bourcigaux N, Simon T, Rousseau G, Finkel L, Benkhalifa M, Christin-Maitre S.
    Hum Reprod; 2008 Jan 01; 23(1):222-6. PubMed ID: 17981816
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  • 18. Chromosome and interphase analysis of placental mosaicism in intrauterine growth retardation.
    Krishnamoorthy A, Gowen LC, Boll KE, Knuppel RA, Sciorra LJ.
    J Perinatol; 1995 Jan 01; 15(1):47-50. PubMed ID: 7650554
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  • 20. Chromosomal heterogeneity of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH).
    Gebhart E, Trautmann U, Reichardt S, Liehr T.
    Anticancer Res; 1993 Jan 01; 13(5C):1857-62. PubMed ID: 8267393
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