These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 7943027)

  • 1. Prediction of mental status in carriers of the fragile X mutation using CGG repeat length.
    Smits A; Smeets D; Hamel B; Dreesen J; de Haan A; van Oost B
    Am J Med Genet; 1994 Jul; 51(4):497-500. PubMed ID: 7943027
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 51(4):490-6. PubMed ID: 7943026
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 325(24):1673-81. PubMed ID: 1944467
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mosaicism in fragile X affected males.
    Nolin SL; Glicksman A; Houck GE; Brown WT; Dobkin CS
    Am J Med Genet; 1994 Jul; 51(4):509-12. PubMed ID: 7943031
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fragile-X carrier females: evidence for a distinct psychopathological phenotype?
    Franke P; Maier W; Hautzinger M; Weiffenbach O; Gänsicke M; Iwers B; Poustka F; Schwab SG; Froster U
    Am J Med Genet; 1996 Aug; 64(2):334-9. PubMed ID: 8844076
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 51(4):463-5. PubMed ID: 7943020
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reliability of diagnostic assessment of normal and premutation status in the fragile X syndrome using DNA testing.
    Fisch GS; Nelson DL; Snow K; Thibodeau SN; Chalifoux M; Holden JJ
    Am J Med Genet; 1994 Jul; 51(4):339-45. PubMed ID: 7942996
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 51(4):471-3. PubMed ID: 7943022
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The emerging fragile X premutation phenotype: evidence from the domain of social cognition.
    Cornish K; Kogan C; Turk J; Manly T; James N; Mills A; Dalton A
    Brain Cogn; 2005 Feb; 57(1):53-60. PubMed ID: 15629215
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [A genetic and molecular study of 85 families affected with the fragile X syndrome].
    Milà Recasens M; Sánchez Díaz A; Glover López G; Castellví Bel S; Carbonell Meseguer P; Kruyer H; Ballesta Martínez F; Estivill Pallejà X
    An Esp Pediatr; 1996 Mar; 44(3):250-6. PubMed ID: 8830601
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Molecular diagnosis and genetic counseling for fragile X mental retardation.
    Pandey UB; Phadke SR; Mittal B
    Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Unstable DNA sequence and methylation in fragile X syndrome].
    Fu SD; Shen Y; Fan Y
    Zhonghua Yi Xue Za Zhi; 1994 Oct; 74(10):611-4, 646-7. PubMed ID: 7842338
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence and instability of fragile X alleles: implications for offering fragile X prenatal diagnosis.
    Cronister A; Teicher J; Rohlfs EM; Donnenfeld A; Hallam S
    Obstet Gynecol; 2008 Mar; 111(3):596-601. PubMed ID: 18310361
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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; 51(4):486-9. PubMed ID: 7943025
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 gene.
    Jenkins EC; Morys I; Henderson J; Genovese M; Carter M; Li SY; Houck GE; Ding X; Stark-Houck SL; Dobkin CS
    Am J Med Genet; 1994 Jul; 51(4):436-42. PubMed ID: 7943013
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Molecular predictors of cognitive involvement in female carriers of fragile X syndrome.
    Taylor AK; Safanda JF; Fall MZ; Quince C; Lang KA; Hull CE; Carpenter I; Staley LW; Hagerman RJ
    JAMA; 1994 Feb; 271(7):507-14. PubMed ID: 8301764
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurobehavioral characteristics of CGG amplification status in fragile X females.
    Thompson NM; Gulley ML; Rogeness GA; Clayton RJ; Johnson C; Hazelton B; Cho CG; Zellmer VT
    Am J Med Genet; 1994 Dec; 54(4):378-83. PubMed ID: 7726212
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A neuropsychological investigation of male premutation carriers of fragile X syndrome.
    Moore CJ; Daly EM; Schmitz N; Tassone F; Tysoe C; Hagerman RJ; Hagerman PJ; Morris RG; Murphy KC; Murphy DG
    Neuropsychologia; 2004; 42(14):1934-47. PubMed ID: 15381024
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Analysis of CGG variation through 642 meioses in Fragile X families.
    Rifé M; Badenas C; Quintó L; Puigoriol E; Tazón B; Rodriguez-Revenga L; Jiménez L; Sánchez A; Milà M
    Mol Hum Reprod; 2004 Oct; 10(10):773-6. PubMed ID: 15322225
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A fragile X male with a broad smear on Southern blot analysis representing 100-500 CGG repeats and no methylation at the EagI site of the FMR-1 gene.
    Lachiewicz AM; Spiridigliozzi GA; McConkie-Rosell A; Burgess D; Feng Y; Warren ST; Tarleton J
    Am J Med Genet; 1996 Aug; 64(2):278-82. PubMed ID: 8844065
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.