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Journal Abstract Search

259 related items for PubMed ID: 7656391

  • 21. 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; 53(3):401-8. PubMed ID: 15750029
    [Abstract] [Full Text] [Related]

  • 22. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report.
    Chang SD, Lin SL, Chen FP, Chu KK.
    J Reprod Med; 1996 Mar; 41(3):175-8. PubMed ID: 8778416
    [Abstract] [Full Text] [Related]

  • 23. Incidence of chromosome numerical changes in multiple myeloma: fluorescence in situ hybridization analysis using 15 chromosome-specific probes.
    Tabernero D, San Miguel JF, Garcia-Sanz M, Nájera L, García-Isidoro M, Peréz-Simon JA, Gonzalez M, Wiegant J, Raap AK, Orfão A.
    Am J Pathol; 1996 Jul; 149(1):153-61. PubMed ID: 8686739
    [Abstract] [Full Text] [Related]

  • 24. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
    Lapierre JM, Cacheux V, Collot N, Da Silva F, Hervy N, Rivet D, Romana S, Wiss J, Benzaken B, Aurias A, Tachdjian G.
    Ann Genet; 1998 Jul; 41(3):133-40. PubMed ID: 9833066
    [Abstract] [Full Text] [Related]

  • 25. [Detection or exclusion of fetal trisomy 18 by in-situ-hybridization of the histologic section].
    Wille S, Mehraein Y.
    Geburtshilfe Frauenheilkd; 1993 Oct; 53(10):684-8. PubMed ID: 8270150
    [Abstract] [Full Text] [Related]

  • 26. [Interphase FISH test as a rapid test for trisomies in amniotic fluid--results of a prospective study].
    Bink K, Pauer HU, Bartels I.
    Z Geburtshilfe Neonatol; 2000 Oct; 204(1):8-13. PubMed ID: 10721180
    [Abstract] [Full Text] [Related]

  • 27. [Clinical application of fluorescence in situ hybridization to prenatal diagnosis].
    Kogame K.
    Rinsho Byori; 1996 Feb; 44(2):141-6. PubMed ID: 8851197
    [Abstract] [Full Text] [Related]

  • 28. Detection of chromosome abnormalities by quantitative fluorescent PCR in ectopic pregnancies.
    Goddijn M, van Stralen M, Schuring-Blom H, Redeker B, van Leeuwen L, Repping S, Leschot N, van der Veen F.
    Gynecol Obstet Invest; 2005 Feb; 60(3):139-44. PubMed ID: 15925891
    [Abstract] [Full Text] [Related]

  • 29. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
    Donaghue C, Mann K, Docherty Z, Ogilvie CM.
    Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
    [Abstract] [Full Text] [Related]

  • 30. [Detection of chromosomal aberration using fluorescence in situ hybridization in DNA diploid colorectal carcinomas].
    Jibiki M, Tagawa Y, Miyashita K, Hara S, Yasutake T, Nakazaki T, Obatake M, Sawai T, Morinaga M, Akama F.
    Gan To Kagaku Ryoho; 1993 Apr; 20(6):759-62. PubMed ID: 8489281
    [Abstract] [Full Text] [Related]

  • 31. Advanced FISH with directly labeled X, Y and 18 DNA probes as a tool for rapid prenatal diagnosis.
    Aviram-Goldring A, Daniely M, Chaki R, Lipitz S, Barkai G, Goldman B.
    J Reprod Med; 1999 Jun; 44(6):497-503. PubMed ID: 10394543
    [Abstract] [Full Text] [Related]

  • 32. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
    Ogilvie CM, Donaghue C, Fox SP, Docherty Z, Mann K.
    J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
    [Abstract] [Full Text] [Related]

  • 33. Chromosome analysis in chorionic villi samples from the first trimester elective terminations.
    Ray M, Manning F, Christie N, Riordan D, Vust A, Wickstrom D.
    Cytobios; 1988 Mar; 55(220):21-31. PubMed ID: 3219884
    [Abstract] [Full Text] [Related]

  • 34. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H, Li H, Wang H, Wang H, Xia Y, Wen J, Long Z, Dai H, Liang D, Xia J, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
    [Abstract] [Full Text] [Related]

  • 35. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).
    Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.
    Prenat Diagn; 2002 Jan; 22(1):29-33. PubMed ID: 11810646
    [Abstract] [Full Text] [Related]

  • 36. Numerical abnormalities of chromosome 7 in human prostate cancer detected by fluorescence in situ hybridization (FISH) on paraffin-embedded tissue sections with centromere-specific DNA probes.
    Zitzelsberger H, Szücs S, Weier HU, Lehmann L, Braselmann H, Enders S, Schilling A, Breul J, Höfler H, Bauchinger M.
    J Pathol; 1994 Apr; 172(4):325-35. PubMed ID: 8207613
    [Abstract] [Full Text] [Related]

  • 37. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
    Suzumori K, Tanemura M, Oya N, Suzumori N, Kim KC, Ohashi H, Fukushima Y.
    Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
    [Abstract] [Full Text] [Related]

  • 38. [Prenatal diagnosis of 95 cases by cytogenetic analysis of early chorionic villi].
    Sun NH.
    Zhonghua Fu Chan Ke Za Zhi; 1987 Mar; 22(2):79-81, 125-6. PubMed ID: 2957181
    [No Abstract] [Full Text] [Related]

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  • 40. Sensitive detection of chromosome copy number aberrations in prostate cancer by fluorescence in situ hybridization.
    Visakorpi T, Hyytinen E, Kallioniemi A, Isola J, Kallioniemi OP.
    Am J Pathol; 1994 Sep; 145(3):624-30. PubMed ID: 8080044
    [Abstract] [Full Text] [Related]

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