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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

62 related items for PubMed ID: 5472949

  • 1. Lack of chromosome aberrations in autism.
    Wolraich M, Bzostek B, Neu RL, Gardner LI.
    N Engl J Med; 1970 Nov 26; 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 26; 40(3):335-45. PubMed ID: 10190335
    [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 26; 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 15; 40(6):457-64. PubMed ID: 8879465
    [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 Sep 15; 36(5):779-91. PubMed ID: 12491987
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No 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 15; 22(3):254-7. PubMed ID: 15952108
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No 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 07; 96(1):15-7. PubMed ID: 10686546
    [Abstract] [Full Text] [Related]

  • 12. Autistic disorder and 22q11.2 duplication.
    Mukaddes NM, Herguner S.
    World J Biol Psychiatry; 2007 Feb 07; 8(2):127-30. PubMed ID: 17455106
    [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 11; 61(2):182-7. PubMed ID: 8669450
    [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 11; 8(2):141-61. PubMed ID: 15165431
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Genetic aspects of infantile autism].
    Lefèvre E, Rivière P, Can Luong L, Duché DJ.
    Sem Hop; 1983 Sep 22; 59(33):2328-32. PubMed ID: 6312601
    [Abstract] [Full Text] [Related]

  • 17. [Genetic studies in autistic disorders].
    Słopień A, Rajewski A.
    Psychiatr Pol; 2000 Sep 22; 34(3):435-46. PubMed ID: 11055182
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [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 25; 74(4):398-411. PubMed ID: 9259376
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.