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 *

115 related articles for article (PubMed ID: 1605236)

  • 1. Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendation.
    Reiss AL; Cianchetti C; Cohen IL; DeVries B; Hagerman R; Hinton V; Froster U; Lachiewicz A; Mazzocco M; Sobesky W
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):61-4. PubMed ID: 1605236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Advances in research on the fragile X syndrome.
    Mazzocco MM
    Ment Retard Dev Disabil Res Rev; 2000; 6(2):96-106. PubMed ID: 10899802
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Neurobiology of Fragile X syndrome: from molecular genetics to neurobehavioral phenotype.
    Kaufmann WE
    Microsc Res Tech; 2002 May; 57(3):131-4. PubMed ID: 12112447
    [No Abstract]   [Full Text] [Related]  

  • 5. Problem solving limitations among cytogenetically expressing fragile X women.
    Mazzocco MM; Hagerman RJ; Pennington BF
    Am J Med Genet; 1992 Apr 15-May 1; 43(1-2):78-86. PubMed ID: 1605239
    [TBL] [Abstract][Full Text] [Related]  

  • 6. DNA testing for fragile X syndrome: implications for parents and family.
    van Rijn MA; de Vries BB; Tibben A; van den Ouweland AM; Halley DJ; Niermeijer MF
    J Med Genet; 1997 Nov; 34(11):907-11. PubMed ID: 9391884
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome.
    Hessl D; Dyer-Friedman J; Glaser B; Wisbeck J; Barajas RG; Taylor A; Reiss AL
    Pediatrics; 2001 Nov; 108(5):E88. PubMed ID: 11694672
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mosaicism for the FMR1 gene influences adaptive skills development in fragile X-affected males.
    Cohen IL; Nolin SL; Sudhalter V; Ding XH; Dobkin CS; Brown WT
    Am J Med Genet; 1996 Aug; 64(2):365-9. PubMed ID: 8844082
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues.
    Mandel JL; Biancalana V
    Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The fragile-X syndrome. On the way to a behavioural phenotype.
    Turk J
    Br J Psychiatry; 1992 Jan; 160():24-35. PubMed ID: 1544010
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fragile X syndrome: a common etiology of mental retardation.
    Rogers RC; Simensen RJ
    Am J Ment Defic; 1987 Mar; 91(5):445-9. PubMed ID: 3565490
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Brief report: aggression and stereotypic behavior in males with fragile X syndrome--moderating secondary genes in a "single gene" disorder.
    Hessl D; Tassone F; Cordeiro L; Koldewyn K; McCormick C; Green C; Wegelin J; Yuhas J; Hagerman RJ
    J Autism Dev Disord; 2008 Jan; 38(1):184-9. PubMed ID: 17340199
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief report.
    Fisch GS; Carpenter N; Howard-Peebles PN; Maddalena A; Simensen R; Tarleton J; Julien-Inalsingh C; Chalifoux M; Holden JJ
    Am J Med Genet; 1996 Aug; 64(2):362-4. PubMed ID: 8844081
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Neurobehavioral phenotype in carriers of the fragile X premutation.
    Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A
    Am J Med Genet; 2001 Nov; 103(4):314-9. PubMed ID: 11746012
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characteristics of fragile X relatives with different attitudes toward terminating an affected pregnancy.
    Meryash DL
    Am J Ment Retard; 1992 Mar; 96(5):528-35. PubMed ID: 1562310
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neuropsychiatry of fragile X-premutation carriers with and without fragile X-associated tremor-ataxia syndrome: implications for neuropsychology.
    Bourgeois JA
    Clin Neuropsychol; 2016 Aug; 30(6):913-28. PubMed ID: 27355575
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.
    Loesch DZ; Bui QM; Grigsby J; Butler E; Epstein J; Huggins RM; Taylor AK; Hagerman RJ
    Neuropsychology; 2003 Oct; 17(4):646-657. PubMed ID: 14599277
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.