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Journal Abstract Search

183 related items for PubMed ID: 2570446

  • 1. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].
    Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M.
    Rev Clin Esp; 1989 Apr; 184(7):364-6. PubMed ID: 2570446
    [Abstract] [Full Text] [Related]

  • 2. Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown families.
    Bridge PJ, Lillicrap DP.
    Am J Med Genet; 1989 May; 33(1):92-9. PubMed ID: 2568753
    [Abstract] [Full Text] [Related]

  • 3. The fragile X syndrome.
    Brown WT.
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [Abstract] [Full Text] [Related]

  • 4. Polymorphic DNA markers in prenatal diagnosis of fragile X syndrome.
    Oberlé I, Mandel JL, Boué J, Mattei MG, Mattei JF.
    Lancet; 1985 Apr 13; 1(8433):871. PubMed ID: 2858726
    [No Abstract] [Full Text] [Related]

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  • 6. [The molecular genetics of the fragile X syndrome. Its molecular diagnosis by DNA probes].
    Giné R, Espinás ML, Antich J, Carballo M.
    Med Clin (Barc); 1992 Feb 01; 98(4):121-4. PubMed ID: 1552760
    [Abstract] [Full Text] [Related]

  • 7. DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3.
    Goonewardena P, Dahl N, Gustavson KH, Holmgren G, Pettersson U.
    Ups J Med Sci Suppl; 1987 Feb 01; 44():155-64. PubMed ID: 2895524
    [Abstract] [Full Text] [Related]

  • 8. [Fragile X syndrome: current knowledge].
    Pellissier MC, Voelckel MA, Mattei JF.
    Pediatrie; 1992 Feb 01; 47(11):743-50. PubMed ID: 1364151
    [Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis in known fragile X carriers.
    Maddalena A, Hicks BD, Spence WC, Levinson G, Howard-Peebles PN.
    Am J Med Genet; 1994 Jul 15; 51(4):490-6. PubMed ID: 7943026
    [Abstract] [Full Text] [Related]

  • 10. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun 15; 27(2):435-48. PubMed ID: 2886048
    [Abstract] [Full Text] [Related]

  • 11. Strategy for reliable prenatal detection of normal male carriers of the fragile X syndrome.
    Halley D, Van Den Ouweland A, Deelen W, Verma I, Oostra B.
    Am J Med Genet; 1994 Jul 15; 51(4):471-3. PubMed ID: 7943022
    [Abstract] [Full Text] [Related]

  • 12. A new DNA probe proximal to and closely linked to fragile X.
    Carpenter NJ, Veenema H, Bakker E, Hofker MH, Pearson PL.
    Am J Med Genet; 1987 Jul 15; 27(3):731-2. PubMed ID: 2888310
    [No Abstract] [Full Text] [Related]

  • 13. Fragile-X syndrome in east Finland: molecular approach to genetic and prenatal diagnosis.
    Ryynänen M, Pulkkinen L, Kirkinen P, Saarikoski S.
    Am J Med Genet; 1994 Jul 15; 51(4):463-5. PubMed ID: 7943020
    [Abstract] [Full Text] [Related]

  • 14. [Use of the polymorphism of flanking DNA probes with respect to the Xq-27 region in a great fragile X pedigree].
    Berriche S, David F, Lucotte G.
    Rev Neurol (Paris); 1989 Jul 15; 145(5):401-5. PubMed ID: 2740689
    [Abstract] [Full Text] [Related]

  • 15. [Mental retardation and the fragile X syndrome].
    Veenema H, Geraedts JP.
    Ned Tijdschr Geneeskd; 1984 Mar 31; 128(13):618-21. PubMed ID: 6717630
    [No Abstract] [Full Text] [Related]

  • 16. [Prenatal diagnosis of hereditary hemoglobinopathies].
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1989 Oct 31; 74(5 Suppl):213-22. PubMed ID: 2574134
    [No Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis and carrier screening for fragile X by PCR.
    Brown WT, Nolin S, Houck G, Ding X, Glicksman A, Li SY, Stark-Houck S, Brophy P, Duncan C, Dobkin C, Jenkins E.
    Am J Med Genet; 1996 Jul 12; 64(1):191-5. PubMed ID: 8826474
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of fragile (X) syndrome.
    Hogge WA, Schonberg SA, Glover TW, Hecht F, Golbus MS.
    Obstet Gynecol; 1984 Mar 12; 63(3 Suppl):19S-21S. PubMed ID: 6700875
    [Abstract] [Full Text] [Related]

  • 19. FRAXA locus in fragile X diagnosis: family studies, prenatal diagnosis, and diagnosis of sporadic cases of mental retardation.
    von Koskull H, Gahmberg N, Salonen R, Salo A, Peippo M.
    Am J Med Genet; 1994 Jul 15; 51(4):486-9. PubMed ID: 7943025
    [Abstract] [Full Text] [Related]

  • 20. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection.
    Dobkin C, Ding X, Li S, Houck G, Nolin SL, Glicksman A, Zhong N, Jenkins EC, Brown WT.
    Am J Med Genet; 1999 Apr 02; 83(4):338-41. PubMed ID: 10208176
    [Abstract] [Full Text] [Related]

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