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Journal Abstract Search

305 related items for PubMed ID: 8826474

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  • 2. 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
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  • 5. Screening for fragile X syndrome.
    Murray J, Cuckle H, Taylor G, Hewison J.
    Health Technol Assess; 1997 Jul 15; 1(4):i-iv, 1-71. PubMed ID: 9414543
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  • 6. Molecular fragile X screening in normal populations.
    Spence WC, Black SH, Fallon L, Maddalena A, Cummings E, Menapace-Drew G, Bick DP, Levinson G, Schulman JD, Howard-Peebles PN.
    Am J Med Genet; 1996 Jul 12; 64(1):181-3. PubMed ID: 8826471
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  • 11. 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
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  • 12. Preconceptional and prenatal screening for fragile X syndrome: experience with 40,000 tests.
    Berkenstadt M, Ries-Levavi L, Cuckle H, Peleg L, Barkai G.
    Prenat Diagn; 2007 Nov 15; 27(11):991-4. PubMed ID: 17705235
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  • 19. Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation.
    Rousseau F, Heitz D, Biancalana V, Blumenfeld S, Kretz C, Boué J, Tommerup N, Van Der Hagen C, DeLozier-Blanchet C, Croquette MF.
    N Engl J Med; 1991 Dec 12; 325(24):1673-81. PubMed ID: 1944467
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  • 20. Identification of small FRAXA premutations.
    Francis D, Burgess T, Mitchell J, Slater H.
    Mol Diagn; 2000 Sep 12; 5(3):221-5. PubMed ID: 11070156
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