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 *

229 related articles for article (PubMed ID: 8844067)

  • 41. Compound heterozygosity at the FMR1 gene.
    Hegde MR; Fawkner M; Chong B; McGaughran J; Gilbert D; Love DR
    Genet Test; 2001; 5(2):135-8. PubMed ID: 11551100
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Screening and instability of FMR1 alleles in a prospective sample of 24,449 mother-newborn pairs from the general population.
    Lévesque S; Dombrowski C; Morel ML; Rehel R; Côté JS; Bussières J; Morgan K; Rousseau F
    Clin Genet; 2009 Dec; 76(6):511-23. PubMed ID: 19863547
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Apparent regression of the CGG repeat in FMR1 to an allele of normal size.
    Vits L; De Boulle K; Reyniers E; Handig I; Darby JK; Oostra B; Willems PJ
    Hum Genet; 1994 Nov; 94(5):523-6. PubMed ID: 7959688
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Decrease in the CGGn trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission.
    Väisänen ML; Haataja R; Leisti J
    Am J Hum Genet; 1996 Sep; 59(3):540-6. PubMed ID: 8751854
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Fragile X syndrome.
    Laxova R
    Adv Pediatr; 1994; 41():305-42. PubMed ID: 7992687
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Haplotype study of intermediate-length alleles at the fragile X (FMR1) gene: ATL1, FMRb, and microsatellite haplotypes differ from those found in common-size FMR1 alleles.
    Curlis Y; Zhang C; Holden JJ; Loesch PK; Mitchell RJ
    Hum Biol; 2005 Feb; 77(1):137-51. PubMed ID: 16114822
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes.
    van den Ouweland AM; Deelen WH; Kunst CB; Uzielli ML; Nelson DL; Warren ST; Oostra BA; Halley DJ
    Hum Mol Genet; 1994 Oct; 3(10):1823-7. PubMed ID: 7849707
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes.
    Zhong N; Ju W; Pietrofesa J; Wang D; Dobkin C; Brown WT
    Am J Med Genet; 1996 Aug; 64(2):261-5. PubMed ID: 8844060
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Fragile X founder chromosomes in Italy: a few initial events and possible explanation for their heterogeneity.
    Chiurazzi P; Genuardi M; Kozak L; Giovannucci-Uzielli ML; Bussani C; Dagna-Bricarelli F; Grasso M; Perroni L; Sebastio G; Sperandeo MP; Oostra BA; Neri G
    Am J Med Genet; 1996 Jul; 64(1):209-15. PubMed ID: 8826478
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Premutation and intermediate-size FMR1 alleles in 10572 males from the general population: loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles.
    Dombrowski C; Lévesque S; Morel ML; Rouillard P; Morgan K; Rousseau F
    Hum Mol Genet; 2002 Feb; 11(4):371-8. PubMed ID: 11854169
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotype.
    Tzeng CC; Tsai LP; Hwu WL; Lin SJ; Chao MC; Jong YJ; Chu SY; Chao WC; Lu CL
    Am J Med Genet A; 2005 Feb; 133A(1):37-43. PubMed ID: 15637705
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Prevalence of carriers of premutation-size alleles of the FMRI gene--and implications for the population genetics of the fragile X syndrome.
    Rousseau F; Rouillard P; Morel ML; Khandjian EW; Morgan K
    Am J Hum Genet; 1995 Nov; 57(5):1006-18. PubMed ID: 7485149
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Advances in molecular analysis of fragile X syndrome.
    Warren ST; Nelson DL
    JAMA; 1994 Feb; 271(7):536-42. PubMed ID: 8301769
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A female compound heterozygote (pre- and full mutation) for the CGG FMR1 expansion.
    Milà M; Castellví-Bel S; Giné R; Vazquez C; Badenas C; Sánchez A; Estivill X
    Hum Genet; 1996 Oct; 98(4):419-21. PubMed ID: 8792815
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus.
    Losekoot M; Hoogendoorn E; Olmer R; Jansen CC; Oosterwijk JC; van den Ouweland AM; Halley DJ; Warren ST; Willemsen R; Oostra BA; Bakker E
    J Med Genet; 1997 Nov; 34(11):924-6. PubMed ID: 9391887
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic.
    Pekarík V; Blazková M; Kozák L
    Am J Med Genet; 1999 May; 84(3):214-6. PubMed ID: 10331594
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Expansion of the CGG repeat in fragile X in the FMR1 gene depends on the sex of the offspring.
    Loesch DZ; Huggins R; Petrovic V; Slater H
    Am J Hum Genet; 1995 Dec; 57(6):1408-13. PubMed ID: 8533771
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Direct mutation analysis of 495 patients for fragile X carrier status/proband diagnosis.
    Kaplan G; Kung M; McClure M; Cronister A
    Am J Med Genet; 1994 Jul; 51(4):501-2. PubMed ID: 7943028
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Fragile X premutations are not a major cause of early menopause.
    Kenneson A; Cramer DW; Warren ST
    Am J Hum Genet; 1997 Dec; 61(6):1362-9. PubMed ID: 9399905
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.