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 *

156 related articles for article (PubMed ID: 2786867)

  • 21. Strengths and weaknesses in the intellectual functioning of males with fragile X syndrome.
    Dykens EM; Hodapp RM; Leckman JF
    Am J Ment Defic; 1987 Sep; 92(2):234-6. PubMed ID: 3434594
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Impact of visual impairment on measures of cognitive function for children with congenital toxoplasmosis: implications for compensatory intervention strategies.
    Roizen N; Kasza K; Karrison T; Mets M; Noble AG; Boyer K; Swisher C; Meier P; Remington J; Jalbrzikowski J; McLeod R; Kipp M; Rabiah P; Chamot D; Estes R; Cezar S; Mack D; Pfiffner L; Stein M; Danis B; Patel D; Hopkins J; Holfels E; Stein L; Withers S; Cameron A; Perkins J; Heydemann P
    Pediatrics; 2006 Aug; 118(2):e379-90. PubMed ID: 16864640
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The fragile X syndrome II: preliminary data on growth and development in males.
    Partington MW
    Am J Med Genet; 1984 Jan; 17(1):175-94. PubMed ID: 6711594
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Intelligence and achievement in children with extra X aneuploidy: a longitudinal perspective.
    Rovet J; Netley C; Bailey J; Keenan M; Stewart D
    Am J Med Genet; 1995 Oct; 60(5):356-63. PubMed ID: 8546146
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Association of insulin-like growth factor I and insulin-like growth factor-binding protein-3 with intelligence quotient among 8- to 9-year-old children in the Avon Longitudinal Study of Parents and Children.
    Gunnell D; Miller LL; Rogers I; Holly JM;
    Pediatrics; 2005 Nov; 116(5):e681-6. PubMed ID: 16263982
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Genotype, molecular phenotype, and cognitive phenotype: correlations in fragile X syndrome.
    Kaufmann WE; Abrams MT; Chen W; Reiss AL
    Am J Med Genet; 1999 Apr; 83(4):286-95. PubMed ID: 10208163
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Adaptive behavior in the fragile X syndrome: profile and development.
    Wiegers AM; Curfs LM; Vermeer EL; Fryns JP
    Am J Med Genet; 1993 Aug; 47(2):216-20. PubMed ID: 8213908
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Fragile X chromosome in normal males.
    Daker MG
    Am J Med Genet; 1983 Apr; 14(4):795-7. PubMed ID: 6846408
    [No Abstract]   [Full Text] [Related]  

  • 31. The greeting behavior of fragile X males.
    Wolff PH; Gardner J; Paccla J; Lappen J
    Am J Ment Retard; 1989 Jan; 93(4):406-11. PubMed ID: 2522786
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled study.
    Cohen IL; Fisch GS; Sudhalter V; Wolf-Schein EG; Hanson D; Hagerman R; Jenkins EC; Brown WT
    Am J Ment Retard; 1988 Mar; 92(5):436-46. PubMed ID: 2965890
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Molecular-neurobehavioral associations in females with the fragile X full mutation.
    Abrams MT; Reiss AL; Freund LS; Baumgardner TL; Chase GA; Denckla MB
    Am J Med Genet; 1994 Jul; 51(4):317-27. PubMed ID: 7942994
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Girls with fragile X syndrome: physical and neurocognitive status and outcome.
    Hagerman RJ; Jackson C; Amiri K; Silverman AC; O'Connor R; Sobesky W
    Pediatrics; 1992 Mar; 89(3):395-400. PubMed ID: 1741210
    [TBL] [Abstract][Full Text] [Related]  

  • 36. High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression.
    Hagerman RJ; Hull CE; Safanda JF; Carpenter I; Staley LW; O'Connor RA; Seydel C; Mazzocco MM; Snow K; Thibodeau SN
    Am J Med Genet; 1994 Jul; 51(4):298-308. PubMed ID: 7942991
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Speech-language and the fragile X syndrome: initial findings.
    Wolf-Schein EG; Sudhalter V; Cohen IL; Fisch GS; Hanson D; Pfadt AG; Hagerman R; Jenkins E; Brown WT
    ASHA; 1987 Jul; 29(7):35-8. PubMed ID: 2956959
    [No Abstract]   [Full Text] [Related]  

  • 38. Facial emotion identification in males with fragile X syndrome.
    Simon EW; Finucane BM
    Am J Med Genet; 1996 Feb; 67(1):77-80. PubMed ID: 8678119
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fragile X boys: evolution of the mental age in childhood. Preliminary data on 10 prepubertal boys.
    Borghgraef M; Swillen A; Van den Berghe H; Fryns JP
    Genet Couns; 1995; 6(2):97-101. PubMed ID: 7546457
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Cognitive and psychiatric variability in three brothers with fragile X syndrome.
    Varley CK; Holm VA; Eren MO
    J Dev Behav Pediatr; 1985 Apr; 6(2):87-90. PubMed ID: 3988946
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.