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 *

162 related articles for article (PubMed ID: 17100202)

  • 1. The velocardiofacial syndrome in older age: dementia and autistic features.
    Evers LJ; Vermaak MP; Engelen JJ; Curfs LM
    Genet Couns; 2006; 17(3):333-40. PubMed ID: 17100202
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autistic disorder and 22q11.2 duplication.
    Mukaddes NM; Herguner S
    World J Biol Psychiatry; 2007; 8(2):127-30. PubMed ID: 17455106
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Neuropsychological profile and neuroimaging in patients with 22Q11.2 Deletion Syndrome: a review.
    Zinkstok J; van Amelsvoort T
    Child Neuropsychol; 2005 Feb; 11(1):21-37. PubMed ID: 15823981
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion).
    Antshel KM; Aneja A; Strunge L; Peebles J; Fremont WP; Stallone K; Abdulsabur N; Higgins AM; Shprintzen RJ; Kates WR
    J Autism Dev Disord; 2007 Oct; 37(9):1776-86. PubMed ID: 17180713
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Annotation: velo-cardio-facial syndrome.
    Murphy KC
    J Child Psychol Psychiatry; 2005 Jun; 46(6):563-71. PubMed ID: 15877762
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology.
    Lajiness-O'Neill R; Beaulieu I; Asamoah A; Titus JB; Bawle E; Ahmad S; Kirk JW; Pollack R
    Arch Clin Neuropsychol; 2006 Feb; 21(2):175-84. PubMed ID: 16307864
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Association of syndromic mental retardation and autism with 22q11.2 duplication.
    Lo-Castro A; Galasso C; Cerminara C; El-Malhany N; Benedetti S; Nardone AM; Curatolo P
    Neuropediatrics; 2009 Jun; 40(3):137-40. PubMed ID: 20020400
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Microduplication 22q11.2 in a child with autism spectrum disorder: clinical and genetic study.
    Ramelli GP; Silacci C; Ferrarini A; Cattaneo C; Visconti P; Pescia G
    Dev Med Child Neurol; 2008 Dec; 50(12):953-5. PubMed ID: 19046189
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 22q11.2 deletion syndrome: introduction.
    Lajiness-O'Neill R
    Child Neuropsychol; 2005 Feb; 11(1):1-3. PubMed ID: 15823979
    [No Abstract]   [Full Text] [Related]  

  • 10. The neurocognitive phenotype in velo-cardio-facial syndrome: a developmental perspective.
    Antshel KM; Fremont W; Kates WR
    Dev Disabil Res Rev; 2008; 14(1):43-51. PubMed ID: 18636636
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome.
    Stiers P; Swillen A; De Smedt B; Lagae L; Devriendt K; D'Agostino E; Sunaert S; Fryns AP
    Child Neuropsychol; 2005 Feb; 11(1):87-108. PubMed ID: 15823985
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
    Sullivan KE
    Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome.
    Gothelf D; Schaer M; Eliez S
    Dev Disabil Res Rev; 2008; 14(1):59-68. PubMed ID: 18636637
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
    Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
    Res Dev Disabil; 2009; 30(4):763-73. PubMed ID: 19070990
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Psychiatric disorders in velo-cardio-facial syndrome].
    Maesen A; Claes SJ; Neyrinck K
    Tijdschr Psychiatr; 2010; 52(1):51-6. PubMed ID: 20054797
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 22q11 deletion syndrome: is that what they used to call . . . ?
    Umlauf MG
    Perspect Psychiatr Care; 2008 Oct; 44(4):259-66. PubMed ID: 18826464
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [DiGeorge syndrome. An underdiagnosed disease category with different clinical features].
    Graesdal A; Surén P; Vadstrup S
    Tidsskr Nor Laegeforen; 2001 Nov; 121(27):3177-9. PubMed ID: 11876140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Cognitive phenotype of velocardiofacial syndrome: a review.
    Furniss F; Biswas AB; Gumber R; Singh N
    Res Dev Disabil; 2011; 32(6):2206-13. PubMed ID: 21764255
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease.
    Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE
    Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951
    [TBL] [Abstract][Full Text] [Related]  

  • 20. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.
    Gothelf D; Eliez S; Thompson T; Hinard C; Penniman L; Feinstein C; Kwon H; Jin S; Jo B; Antonarakis SE; Morris MA; Reiss AL
    Nat Neurosci; 2005 Nov; 8(11):1500-2. PubMed ID: 16234808
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.