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Journal Abstract Search

159 related items for PubMed ID: 7847930

  • 1. [Applications of fluorescence in situ hybridization in prenatal diagnosis].
    Pescia G, Fokstuen S, Thonney F.
    Arch Gynecol Obstet; 1994; 255 Suppl 2():S367-71. PubMed ID: 7847930
    [No Abstract] [Full Text] [Related]

  • 2. Amniocentesis and prenatal detection of genetic disease.
    Finley SC.
    J Med Assoc State Ala; 1979 Feb; 48(8):16-7. PubMed ID: 45593
    [No Abstract] [Full Text] [Related]

  • 3. [Prenatal screening for abnormalities and chromosomal disorders].
    Brandt NJ, Skovby F.
    Ugeskr Laeger; 1996 Feb 26; 158(9):1197. PubMed ID: 8644422
    [No Abstract] [Full Text] [Related]

  • 4. [Methods and indications for prenatal diagnosis. I. Elements of human genetics].
    Masse A.
    Union Med Can; 1983 Aug 26; 112(8):708-10, 712-3, 721. PubMed ID: 6636360
    [No Abstract] [Full Text] [Related]

  • 5. [Indications for chromosome analysis].
    Passarge E.
    Internist (Berl); 1978 Aug 26; 19(8):445-51. PubMed ID: 357333
    [No Abstract] [Full Text] [Related]

  • 6. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].
    Ulmer R, Pfeiffer RA, Kollert A, Beinder E.
    Z Geburtshilfe Neonatol; 2000 Aug 26; 204(1):1-7. PubMed ID: 10721179
    [Abstract] [Full Text] [Related]

  • 7. Antenatal diagnosis.
    Maidman JE.
    Obstet Gynecol Annu; 1972 Aug 26; 1():65-101. PubMed ID: 4591074
    [No Abstract] [Full Text] [Related]

  • 8. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
    Huang Y, Sun X, Li Q.
    Zhonghua Fu Chan Ke Za Zhi; 1999 Mar 26; 34(3):153-5. PubMed ID: 11263185
    [Abstract] [Full Text] [Related]

  • 9. [Current state of prenatal genetic diagnosis].
    Schmid W.
    Schweiz Rundsch Med Prax; 1984 Feb 21; 73(8):239-43. PubMed ID: 6200909
    [No Abstract] [Full Text] [Related]

  • 10. The antenatal detection of genetic disorders. Current status and future prospects.
    Golbus MS.
    Obstet Gynecol; 1976 Oct 21; 48(4):497-506. PubMed ID: 135214
    [No Abstract] [Full Text] [Related]

  • 11. [Identification of Y chromosome material in an XX male by means of fluorescent in situ hybridization].
    Brandt CA, Hindkjaer J, Strømkjaer H, Christensen MF, Kølvraa S.
    Ugeskr Laeger; 1992 Nov 16; 154(47):3321-4. PubMed ID: 1462437
    [Abstract] [Full Text] [Related]

  • 12. [Fetal chromosome abnormalities diagnosed by chorionic villi sampling].
    Gardó S, Bajnóczky K, Nagy M, Nagy S.
    Orv Hetil; 1993 Oct 31; 134(44):2427-30. PubMed ID: 8233461
    [Abstract] [Full Text] [Related]

  • 13. Prenatal genetic diagnosis: nine years experience.
    Henry GP, Peakman DC, Robinson A.
    Obstet Gynecol Surv; 1978 Sep 31; 33(9):569-77. PubMed ID: 80771
    [Abstract] [Full Text] [Related]

  • 14. Prenatal cytogenetic abnormalities: correlations of structural rearrangements and ultrasonographically detected fetal anomalies.
    Hume RF, Kilmer-Ernst P, Wolfe HM, Ebrahim SA, Treadwell MC, Johnson MP, Evans MI.
    Am J Obstet Gynecol; 1995 Oct 31; 173(4):1334-6. PubMed ID: 7485349
    [Abstract] [Full Text] [Related]

  • 15. [Development of an original computer program FISHMet: use for molecular cytogenetic diagnosis and genome mapping by fluorescent in situ hybridization (FISH)].
    Iurov IuB, Khazatskiĭ IA, Akindinov VA, Dovgilov LV, Kobrinskiĭ BA, Vorsanova SG.
    Klin Lab Diagn; 2000 Aug 31; (8):34-6. PubMed ID: 11031430
    [Abstract] [Full Text] [Related]

  • 16. The origin of genetic defects in the human and their detection in the preimplantation embryo.
    Delhanty JD, Handyside AH.
    Hum Reprod Update; 1995 May 31; 1(3):201-15. PubMed ID: 9187939
    [No Abstract] [Full Text] [Related]

  • 17. [Molecular cytogenetic pre- and postnatal diagnosis of chromosomal abnormalities].
    Vorsanova SG, Iurov IuB.
    Vestn Ross Akad Med Nauk; 1999 May 31; (11):12-5. PubMed ID: 10635746
    [Abstract] [Full Text] [Related]

  • 18. Cytogenetics of müllerian agenesis. A case report.
    Jaffe SB, Loucopoulos A, Jewelewicz R.
    J Reprod Med; 1992 Mar 31; 37(3):242-6. PubMed ID: 1564711
    [Abstract] [Full Text] [Related]

  • 19. [Chromosome aberrations in fetuses and neonates].
    Boczkowski K.
    Postepy Hig Med Dosw; 1981 Mar 31; 34(6):479-89. PubMed ID: 7291083
    [No Abstract] [Full Text] [Related]

  • 20. Rapid aneuploid diagnosis of high-risk fetuses by fluorescence in situ hybridization.
    Lapidot-Lifson Y, Lebo RV, Flandermeyer RR, Chung JH, Golbus MS.
    Am J Obstet Gynecol; 1996 Mar 31; 174(3):886-90. PubMed ID: 8633662
    [Abstract] [Full Text] [Related]

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