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 *

132 related articles for article (PubMed ID: 16556609)

  • 1. An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene cluster.
    Vincent JB; Horike SI; Choufani S; Paterson AD; Roberts W; Szatmari P; Weksberg R; Fernandez B; Scherer SW
    J Med Genet; 2006 May; 43(5):429-34. PubMed ID: 16556609
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Association between a GABRB3 polymorphism and autism.
    Buxbaum JD; Silverman JM; Smith CJ; Greenberg DA; Kilifarski M; Reichert J; Cook EH; Fang Y; Song CY; Vitale R
    Mol Psychiatry; 2002; 7(3):311-6. PubMed ID: 11920158
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic studies of autistic disorder and chromosome 7.
    Ashley-Koch A; Wolpert CM; Menold MM; Zaeem L; Basu S; Donnelly SL; Ravan SA; Powell CM; Qumsiyeh MB; Aylsworth AS; Vance JM; Gilbert JR; Wright HH; Abramson RK; DeLong GR; Cuccaro ML; Pericak-Vance MA
    Genomics; 1999 Nov; 61(3):227-36. PubMed ID: 10552924
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. 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]  

  • 8. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unexpected identification of two interstitial deletions in a patient with a pericentric inversion of a chromosome 4 and an abnormal phenotype.
    Piovani G; Borsani G; Bertini V; Kalscheuer VM; Viertel P; Bellotti D; Valseriati D; Barlati S
    Eur J Med Genet; 2006; 49(3):215-23. PubMed ID: 16762823
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Possible association between the androgen receptor gene and autism spectrum disorder.
    Henningsson S; Jonsson L; Ljunggren E; Westberg L; Gillberg C; Råstam M; Anckarsäter H; Nygren G; Landén M; Thuresson K; Betancur C; Leboyer M; Gillberg C; Eriksson E; Melke J
    Psychoneuroendocrinology; 2009 Jun; 34(5):752-61. PubMed ID: 19167832
    [TBL] [Abstract][Full Text] [Related]  

  • 11. No association between the ryanodine receptor 3 gene and autism in a Japanese population.
    Tochigi M; Kato C; Ohashi J; Koishi S; Kawakubo Y; Yamamoto K; Matsumoto H; Hashimoto O; Kim SY; Watanabe K; Kano Y; Nanba E; Kato N; Sasaki T
    Psychiatry Clin Neurosci; 2008 Jun; 62(3):341-4. PubMed ID: 18588595
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Pericentric inversion inv(7)(p11q21.1): report on two cases and genotype-phenotype correlations.
    Vorsanova SG; Iourov IY; Demidova IA; Kolotii AD; Soloviev IV; Yurov YB
    Tsitol Genet; 2006; 40(3):45-8. PubMed ID: 16933852
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindred.
    Hirsch B; Baldinger S
    Am J Med Genet; 1993 Jan; 45(1):5-8. PubMed ID: 8418660
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility.
    Cukier HN; Skaar DA; Rayner-Evans MY; Konidari I; Whitehead PL; Jaworski JM; Cuccaro ML; Pericak-Vance MA; Gilbert JR
    Autism Res; 2009 Oct; 2(5):258-66. PubMed ID: 19877165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Autism and Williams syndrome: a case report.
    Herguner S; Mukaddes NM
    World J Biol Psychiatry; 2006; 7(3):186-8. PubMed ID: 16861145
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Recombinant 4 syndrome due to an unbalanced pericentric inversion of chromosome 4.
    Battaglia A; Brothman AR; Carey JC
    Am J Med Genet; 2002 Sep; 112(1):103-6. PubMed ID: 12239731
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Examination of AVPR1a as an autism susceptibility gene.
    Wassink TH; Piven J; Vieland VJ; Pietila J; Goedken RJ; Folstein SE; Sheffield VC
    Mol Psychiatry; 2004 Oct; 9(10):968-72. PubMed ID: 15098001
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.