BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

109 related articles for article (PubMed ID: 18183041)

  • 1. A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
    Gilling M; Lauritsen MB; Møller M; Henriksen KF; Vicente A; Oliveira G; Cintin C; Eiberg H; Andersen PS; Mors O; Rosenberg T; Brøndum-Nielsen K; Cotterill RM; Lundsteen C; Ropers HH; Ullmann R; Bache I; Tümer Z; Tommerup N
    Eur J Hum Genet; 2008 Mar; 16(3):312-9. PubMed ID: 18183041
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification and molecular characterization of two novel chromosomal deletions associated with autism.
    Chien WH; Gau SS; Wu YY; Huang YS; Fang JS; Chen YJ; Soong WT; Chiu YN; Chen CH
    Clin Genet; 2010 Nov; 78(5):449-56. PubMed ID: 20236125
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent 16p11.2 microdeletions in autism.
    Kumar RA; KaraMohamed S; Sudi J; Conrad DF; Brune C; Badner JA; Gilliam TC; Nowak NJ; Cook EH; Dobyns WB; Christian SL
    Hum Mol Genet; 2008 Feb; 17(4):628-38. PubMed ID: 18156158
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Autism-associated familial microdeletion of Xp11.22.
    Qiao Y; Liu X; Harvard C; Hildebrand MJ; Rajcan-Separovic E; Holden JJ; Lewis ME
    Clin Genet; 2008 Aug; 74(2):134-44. PubMed ID: 18498374
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Characterization of 11p14-p12 deletion in WAGR syndrome by array CGH for identifying genes contributing to mental retardation and autism.
    Xu S; Han JC; Morales A; Menzie CM; Williams K; Fan YS
    Cytogenet Genome Res; 2008; 122(2):181-7. PubMed ID: 19096215
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two patients with balanced translocations and autistic disorder: CSMD3 as a candidate gene for autism found in their common 8q23 breakpoint area.
    Floris C; Rassu S; Boccone L; Gasperini D; Cao A; Crisponi L
    Eur J Hum Genet; 2008 Jun; 16(6):696-704. PubMed ID: 18270536
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Autism: an overview of genetic aetiology.
    Bayou N; M'rad R; Ahlem B; Béchir Helayem M; Chaabouni H
    Tunis Med; 2008 Jun; 86(6):573-8. PubMed ID: 19216451
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
    Wang P; Carrion P; Qiao Y; Tyson C; Hrynchak M; Calli K; Lopez-Rangel E; Andrieux J; Delobel B; Duban-Bedu B; Thuresson AC; Annerén G; Liu X; Rajcan-Separovic E; Suzanne Lewis ME
    Eur J Med Genet; 2013 Aug; 56(8):420-5. PubMed ID: 23727450
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular cloning and analysis of breakpoints on ring chromosome 17 in a patient with autism.
    Vazna A; Havlovicova M; Sedlacek Z
    Gene; 2008 Jan; 407(1-2):186-92. PubMed ID: 17996402
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A 12Mb deletion at 7q33-q35 associated with autism spectrum disorders and primary amenorrhea.
    Rossi E; Verri AP; Patricelli MG; Destefani V; Ricca I; Vetro A; Ciccone R; Giorda R; Toniolo D; Maraschio P; Zuffardi O
    Eur J Med Genet; 2008; 51(6):631-8. PubMed ID: 18675947
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number changes of the microcephalin 1 gene (MCPH1) in patients with autism spectrum disorders.
    Ozgen HM; van Daalen E; Bolton PF; Maloney VK; Huang S; Cresswell L; van den Boogaard MJ; Eleveld MJ; van 't Slot R; Hochstenbach R; Beemer FA; Barrow M; Barber JC; Poot M
    Clin Genet; 2009 Oct; 76(4):348-56. PubMed ID: 19793310
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A complex chromosome rearrangement in a boy with autism.
    Lopreiato JO; Wulfsberg EA
    J Dev Behav Pediatr; 1992 Aug; 13(4):281-3. PubMed ID: 1506468
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
    Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
    Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism.
    Castermans D; Vermeesch JR; Fryns JP; Steyaert JG; Van de Ven WJ; Creemers JW; Devriendt K
    Eur J Hum Genet; 2007 Apr; 15(4):422-31. PubMed ID: 17290275
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
    Vincent JB; Choufani S; Horike S; Stachowiak B; Li M; Dill FJ; Marshall C; Hrynchak M; Pewsey E; Ukadike KC; Friedman JM; Srivastava AK; Scherer SW
    Psychiatr Genet; 2008 Jun; 18(3):101-9. PubMed ID: 18496206
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics of childhood disorders: XLVII. Autism, part 6: duplication and inherited susceptibility of chromosome 15q11-q13 genes in autism.
    Sutcliffe JS; Nurmi EL; Lombroso PJ
    J Am Acad Child Adolesc Psychiatry; 2003 Feb; 42(2):253-6. PubMed ID: 12544187
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. The search for autism disease genes.
    Wassink TH; Brzustowicz LM; Bartlett CW; Szatmari P
    Ment Retard Dev Disabil Res Rev; 2004; 10(4):272-83. PubMed ID: 15666342
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cytogenetic, FISH and array-CGH characterization of a complex chromosomal rearrangement carried by a mentally and language impaired patient.
    Ballarati L; Recalcati MP; Bedeschi MF; Lalatta F; Valtorta C; Bellini M; Finelli P; Larizza L; Giardino D
    Eur J Med Genet; 2009; 52(4):218-23. PubMed ID: 19236961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.