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 *

110 related articles for article (PubMed ID: 1458226)

  • 21. Fragile X syndrome.
    Reiss AL; Freund L
    Biol Psychiatry; 1990 Jan; 27(2):223-40. PubMed ID: 2403814
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Molecular analysis of Fragile X syndrome.
    Basehore MJ; Friez MJ
    Curr Protoc Hum Genet; 2009 Oct; Chapter 9():Unit 9.5. PubMed ID: 19806593
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Fragile site X chromosomes in mentally retarded boys.
    Moon HR; Moon SY
    J Korean Med Sci; 1993 Jun; 8(3):192-6. PubMed ID: 8240748
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation].
    Aspillaga M; Jara L; Avendaño I; López M
    Rev Med Chil; 1998 Dec; 126(12):1447-54. PubMed ID: 10349158
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [DNA diagnosis of fragile X syndrome in a family. A new type of heredity--dynamic mutations].
    Eiken HG; Boman H; Apold J
    Tidsskr Nor Laegeforen; 1993 Oct; 113(26):3236-9. PubMed ID: 8236216
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Fragile X syndrome.
    Terracciano A; Chiurazzi P; Neri G
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):32-7. PubMed ID: 16010677
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Psychiatric and autistic comorbidity in fragile X syndrome across ages.
    Gabis LV; Baruch YK; Jokel A; Raz R
    J Child Neurol; 2011 Aug; 26(8):940-8. PubMed ID: 21527394
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The fragile X syndrome.
    de Vries BB; Halley DJ; Oostra BA; Niermeijer MF
    J Med Genet; 1998 Jul; 35(7):579-89. PubMed ID: 9678703
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotype.
    Warren ST
    Am J Med Genet; 1988; 30(1-2):681-8. PubMed ID: 3177478
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fragile X-syndrome: literature review and report of two cases.
    Ridaura-Ruiz L; Quinteros-Borgarello M; Berini-Aytés L; Gay-Escoda C
    Med Oral Patol Oral Cir Bucal; 2009 Sep; 14(9):e434-9. PubMed ID: 19718005
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Fragile X syndrome among children with mental retardation.
    Elango R; Verma IC
    Indian J Pediatr; 1996; 63(4):533-8. PubMed ID: 10832474
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Effect of folic acid treatment in the fragile X syndrome.
    Gustavson KH; Dahlbom K; Flood A; Holmgren G; Blomquist HK; Sanner G
    Clin Genet; 1985 May; 27(5):463-7. PubMed ID: 4006270
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Behavioral relationship between autism and fragile x syndrome.
    Demark JL; Feldman MA; Holden JJ
    Am J Ment Retard; 2003 Sep; 108(5):314-26. PubMed ID: 12901707
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The fragile X syndrome: implications of molecular genetics for the clinical syndrome.
    Rousseau F
    Eur J Clin Invest; 1994 Jan; 24(1):1-10. PubMed ID: 8187801
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Standards for selected anthropometric measurements in males with the fragile X syndrome.
    Butler MG; Brunschwig A; Miller LK; Hagerman RJ
    Pediatrics; 1992 Jun; 89(6 Pt 1):1059-62. PubMed ID: 1594348
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Fragile X Syndrome: Introduction.
    Reches A
    Methods Mol Biol; 2019; 1942():3-10. PubMed ID: 30900171
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Two brothers with mental retardation discordant for the fragile-X syndrome.
    Van Roy BC; Willems PJ; Vits LJ; Ceulemans BP; Coucke PJ; Van der Auwera BJ; Lormans JA; Dumon JE
    Am J Med Genet; 1990 May; 36(1):122-5. PubMed ID: 2333901
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Molecular pathology of the fragile X syndrome.
    Tsongalis GJ; Silverman LM
    Arch Pathol Lab Med; 1993 Nov; 117(11):1121-5. PubMed ID: 8239933
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. A homogeneous assay for analysis of FMR1 promoter methylation in patients with fragile X syndrome.
    Dahl C; Grønskov K; Larsen LA; Guldberg P; Brøndum-Nielsen K
    Clin Chem; 2007 Apr; 53(4):790-3. PubMed ID: 17259243
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.