BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

66 related articles for article (PubMed ID: 5472949)

  • 1. Lack of chromosome aberrations in autism.
    Wolraich M; Bzostek B; Neu RL; Gardner LI
    N Engl J Med; 1970 Nov; 283(22):1231. PubMed ID: 5472949
    [No Abstract]   [Full Text] [Related]  

  • 2. Infantile autism and associated autosomal chromosome abnormalities: a register-based study and a literature survey.
    Lauritsen M; Mors O; Mortensen PB; Ewald H
    J Child Psychol Psychiatry; 1999 Mar; 40(3):335-45. PubMed ID: 10190335
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fragile X syndrome associated with Tourette symptomatology in a male with moderate mental retardation and autism.
    Kerbeshian J; Burd L; Martsolf JT
    J Dev Behav Pediatr; 1984 Aug; 5(4):201-3. PubMed ID: 6590572
    [No Abstract]   [Full Text] [Related]  

  • 4. X chromosome and infantile autism.
    Petit E; Hérault J; Raynaud M; Cherpi C; Perrot A; Barthélémy C; Lelord G; Müh JP
    Biol Psychiatry; 1996 Sep; 40(6):457-64. PubMed ID: 8879465
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Evaluation of q11-q13 locus of chromosome 15 aberrations and polymorphisms in the B3 subunit of the GABA-A receptor gene (GABRB3) in autistic patients].
    Słopień A; Rajewski A; Budny B; Czerski P
    Psychiatr Pol; 2002; 36(5):779-91. PubMed ID: 12491987
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sex chromosome abnormalities in autistic children--long Y chromosome.
    Hoshino Y; Yashima Y; Tachibana R; Kaneko M; Watanabe M; Kumashiro H
    Fukushima J Med Sci; 1979; 26(1-2):31-42. PubMed ID: 521003
    [No Abstract]   [Full Text] [Related]  

  • 7. Clinical and cytogenetic manifestations of subtelomeric aberrations: Report of six cases.
    Font-Montgomery E; Weaver DD; Walsh L; Christensen C; Thurston VC
    Birth Defects Res A Clin Mol Teratol; 2004 Jun; 70(6):408-15. PubMed ID: 15211711
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ring chromosome 22 and autism: report and review.
    MacLean JE; Teshima IE; Szatmari P; Nowaczyk MJ
    Am J Med Genet; 2000 Feb; 90(5):382-5. PubMed ID: 10706359
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of chromosome aberrations in Chinese children with autism using G-banding and BAC FISH.
    Liu QJ; Ma F; Li D; Wang XW; Tian WY; Chen Y; Feng JB; Lu X; Chen DQ; Chen XN; Shen Y
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):254-7. PubMed ID: 15952108
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorder.
    Lukusa T; Vermeesch JR; Holvoet M; Fryns JP; Devriendt K
    Genet Couns; 2004; 15(3):293-301. PubMed ID: 15517821
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium.
    Ogilvie CM; Moore J; Daker M; Palferman S; Docherty Z
    Am J Med Genet; 2000 Feb; 96(1):15-7. PubMed ID: 10686546
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation.
    Flejter WL; Bennett-Baker PE; Ghaziuddin M; McDonald M; Sheldon S; Gorski JL
    Am J Med Genet; 1996 Jan; 61(2):182-7. PubMed ID: 8669450
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Chromosomal anomalies in individuals with autism: a strategy towards the identification of genes involved in autism.
    Castermans D; Wilquet V; Steyaert J; Van de Ven W; Fryns JP; Devriendt K
    Autism; 2004 Jun; 8(2):141-61. PubMed ID: 15165431
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Chromosome 15q11-13 region and the autistic disorder.
    Sabry MA; Farag TI
    J Intellect Disabil Res; 1998 Jun; 42 ( Pt 3)():259. PubMed ID: 9678411
    [No Abstract]   [Full Text] [Related]  

  • 16. [Genetic aspects of infantile autism].
    Lefèvre E; Rivière P; Can Luong L; Duché DJ
    Sem Hop; 1983 Sep; 59(33):2328-32. PubMed ID: 6312601
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic studies in autistic disorders].
    Słopień A; Rajewski A
    Psychiatr Pol; 2000; 34(3):435-46. PubMed ID: 11055182
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism.
    Salmon B; Hallmayer J; Rogers T; Kalaydjieva L; Petersen PB; Nicholas P; Pingree C; McMahon W; Spiker D; Lotspeich L; Kraemer H; McCague P; Dimiceli S; Nouri N; Pitts T; Yang J; Hinds D; Myers RM; Risch N
    Am J Med Genet; 1999 Oct; 88(5):551-6. PubMed ID: 10490715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Fragile X chromosome and autistic mental retardation. Apropos of 23 cases].
    Bénézech M; Noel B; Noel L; Bourgeois M
    Ann Med Psychol (Paris); 1983 Nov; 141(9):1006-11. PubMed ID: 6666917
    [No Abstract]   [Full Text] [Related]  

  • 20. Personality and language characteristics in parents from multiple-incidence autism families.
    Piven J; Palmer P; Landa R; Santangelo S; Jacobi D; Childress D
    Am J Med Genet; 1997 Jul; 74(4):398-411. PubMed ID: 9259376
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.