BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

166 related articles for article (PubMed ID: 17318841)

  • 1. Behavioral problems in relation to intelligence in children with 22q11.2 deletion syndrome: a matched control study.
    Jansen PW; Duijff SN; Beemer FA; Vorstman JA; Klaassen PW; Morcus ME; Heineman-de Boer JA
    Am J Med Genet A; 2007 Mar; 143A(6):574-80. PubMed ID: 17318841
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sex differences in the behavior of children with the 22q11 deletion syndrome.
    Sobin C; Kiley-Brabeck K; Monk SH; Khuri J; Karayiorgou M
    Psychiatry Res; 2009 Mar; 166(1):24-34. PubMed ID: 19217670
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Behavior in preschool children with the 22q11.2 deletion syndrome.
    Klaassen P; Duijff S; Swanenburg de Veye H; Vorstman J; Beemer F; Sinnema G
    Am J Med Genet A; 2013 Jan; 161A(1):94-101. PubMed ID: 23239609
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school age.
    Swillen A; Devriendt K; Ghesquière P; Fryns JP
    Genet Couns; 2001; 12(4):309-17. PubMed ID: 11837599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [22q11.2 microdeletion].
    Schneider M; Eliez S
    Arch Pediatr; 2010 Apr; 17(4):431-4. PubMed ID: 19942416
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cognitive and behavioral trajectories in 22q11DS from childhood into adolescence: a prospective 6-year follow-up study.
    Duijff SN; Klaassen PW; Swanenburg de Veye HF; Beemer FA; Sinnema G; Vorstman JA
    Res Dev Disabil; 2013 Sep; 34(9):2937-45. PubMed ID: 23816629
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A review of neurocognitive and behavioral profiles associated with 22q11 deletion syndrome: implications for clinical evaluation and treatment.
    Ousley O; Rockers K; Dell ML; Coleman K; Cubells JF
    Curr Psychiatry Rep; 2007 Apr; 9(2):148-58. PubMed ID: 17389127
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Chromosome 22q11 deletion syndrome and its relevance for child and adolescent psychiatry. An overview of etiology, physical symptoms, aspects of child development and psychiatric disorders].
    Briegel W; Cohen M
    Z Kinder Jugendpsychiatr Psychother; 2004 May; 32(2):107-15. PubMed ID: 15181786
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology.
    Sinderberry B; Brown S; Hammond P; Stevens AF; Schall U; Murphy DG; Murphy KC; Campbell LE
    Res Dev Disabil; 2013 Jan; 34(1):116-25. PubMed ID: 22940165
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microduplication 22q11.2: a description of the clinical, developmental and behavioral characteristics during childhood.
    Van Campenhout S; Devriendt K; Breckpot J; Frijns JP; Peeters H; Van Buggenhout G; Van Esch H; Maes B; Swillen A
    Genet Couns; 2012; 23(2):135-48. PubMed ID: 22876571
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 22q11 deletion syndrome (CATCH 22): neuropsychiatric and neuropsychological aspects.
    Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
    Dev Med Child Neurol; 2002 Jan; 44(1):44-50. PubMed ID: 11811651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Thyroid gland and carotid artery anomalies in 22q11.2 deletion syndromes.
    de Almeida JR; James AL; Papsin BC; Weksburg R; Clark H; Blaser S
    Laryngoscope; 2009 Aug; 119(8):1495-500. PubMed ID: 19507237
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Manic symptoms and behavioral dysregulation in youth with velocardiofacial syndrome (22q11.2 deletion syndrome).
    Aneja A; Fremont WP; Antshel KM; Faraone SV; AbdulSabur N; Higgins AM; Shprintzen R; Kates WR
    J Child Adolesc Psychopharmacol; 2007 Feb; 17(1):105-14. PubMed ID: 17343558
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 22q11.2 deletion syndrome: behaviour problems of infants and parental stress.
    Briegel W; Schneider M; Schwab KO
    Child Care Health Dev; 2007 May; 33(3):319-24. PubMed ID: 17439446
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome.
    Hooper SR; Curtiss K; Schoch K; Keshavan MS; Allen A; Shashi V
    Res Dev Disabil; 2013 May; 34(5):1758-69. PubMed ID: 23506790
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Intelligence and visual motor integration in 5-year-old children with 22q11-deletion syndrome.
    Duijff S; Klaassen P; Beemer F; Swanenburg de Veye H; Vorstman J; Sinnema G
    Res Dev Disabil; 2012; 33(2):334-40. PubMed ID: 22119678
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Discrepancies in parent and teacher ratings of social-behavioral functioning of children with chromosome 22q11.2 deletion syndrome: implications for assessment.
    Wray E; Shashi V; Schoch K; Curtiss K; Hooper SR
    Am J Intellect Dev Disabil; 2013 Sep; 118(5):339-52. PubMed ID: 24245728
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion.
    Klaassen P; Duijff S; Swanenburg de Veye H; Beemer F; Sinnema G; Breetvelt E; Schappin R; Vorstman J
    Am J Med Genet B Neuropsychiatr Genet; 2016 Sep; 171(6):790-6. PubMed ID: 26953189
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A comparative study of cognition and brain anatomy between two neurodevelopmental disorders: 22q11.2 deletion syndrome and Williams syndrome.
    Campbell LE; Stevens A; Daly E; Toal F; Azuma R; Karmiloff-Smith A; Murphy DG; Murphy KC
    Neuropsychologia; 2009 Mar; 47(4):1034-44. PubMed ID: 19061904
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.
    Shashi V; Keshavan M; Kaczorowski J; Schoch K; Lewandowski KE; McConkie-Rosell A; Hooper SR; Kwapil TR
    J Genet Couns; 2010 Oct; 19(5):535-44. PubMed ID: 20680421
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.