156 related articles for article (PubMed ID: 10889047)
1. Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual.
Vincent JB; Herbrick JA; Gurling HM; Bolton PF; Roberts W; Scherer SW
Am J Hum Genet; 2000 Aug; 67(2):510-4. PubMed ID: 10889047
[TBL] [Abstract][Full Text] [Related]
2. A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: molecular analysis of the chromosome 7 breakpoint.
Tentler D; Brandberg G; Betancur C; Gillberg C; Annerén G; Orsmark C; Green ED; Carlsson B; Dahl N
Am J Med Genet; 2001 Dec; 105(8):729-36. PubMed ID: 11803521
[TBL] [Abstract][Full Text] [Related]
3. The RAY1/ST7 tumor-suppressor locus on chromosome 7q31 represents a complex multi-transcript system.
Vincent JB; Petek E; Thevarkunnel S; Kolozsvari D; Cheung J; Patel M; Scherer SW
Genomics; 2002 Sep; 80(3):283-94. PubMed ID: 12213198
[TBL] [Abstract][Full Text] [Related]
4. Chromosome 7q: where autism meets language disorder?
Folstein SE; Mankoski RE
Am J Hum Genet; 2000 Aug; 67(2):278-81. PubMed ID: 10889044
[No Abstract] [Full Text] [Related]
5. The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
Lai CS; Fisher SE; Hurst JA; Levy ER; Hodgson S; Fox M; Jeremiah S; Povey S; Jamison DC; Green ED; Vargha-Khadem F; Monaco AP
Am J Hum Genet; 2000 Aug; 67(2):357-68. PubMed ID: 10880297
[TBL] [Abstract][Full Text] [Related]
6. Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome.
Petek E; Windpassinger C; Vincent JB; Cheung J; Boright AP; Scherer SW; Kroisel PM; Wagner K
Am J Hum Genet; 2001 Apr; 68(4):848-58. PubMed ID: 11254443
[TBL] [Abstract][Full Text] [Related]
7. Sorting nexin 3 (SNX3) is disrupted in a patient with a translocation t(6;13)(q21;q12) and microcephaly, microphthalmia, ectrodactyly, prognathism (MMEP) phenotype.
Vervoort VS; Viljoen D; Smart R; Suthers G; DuPont BR; Abbott A; Schwartz CE
J Med Genet; 2002 Dec; 39(12):893-9. PubMed ID: 12471201
[TBL] [Abstract][Full Text] [Related]
8. Identification of the human cortactin-binding protein-2 gene from the autism candidate region at 7q31.
Cheung J; Petek E; Nakabayashi K; Tsui LC; Vincent JB; Scherer SW
Genomics; 2001 Nov; 78(1-2):7-11. PubMed ID: 11707066
[TBL] [Abstract][Full Text] [Related]
9. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31.
Warburton P; Baird G; Chen W; Morris K; Jacobs BW; Hodgson S; Docherty Z
Am J Med Genet; 2000 Apr; 96(2):228-34. PubMed ID: 10893502
[TBL] [Abstract][Full Text] [Related]
10. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Sultana R; Yu CE; Yu J; Munson J; Chen D; Hua W; Estes A; Cortes F; de la Barra F; Yu D; Haider ST; Trask BJ; Green ED; Raskind WH; Disteche CM; Wijsman E; Dawson G; Storm DR; Schellenberg GD; Villacres EC
Genomics; 2002 Aug; 80(2):129-34. PubMed ID: 12160723
[TBL] [Abstract][Full Text] [Related]
11. The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour.
Vernon EG; Malik K; Reynolds P; Powlesland R; Dallosso AR; Jackson S; Henthorn K; Green ED; Brown KW
Oncogene; 2003 Mar; 22(9):1371-80. PubMed ID: 12618763
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Linkage and association of the mitochondrial aspartate/glutamate carrier SLC25A12 gene with autism.
Ramoz N; Reichert JG; Smith CJ; Silverman JM; Bespalova IN; Davis KL; Buxbaum JD
Am J Psychiatry; 2004 Apr; 161(4):662-9. PubMed ID: 15056512
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: identification of a BAC contig spanning the translocation breakpoint at 7q21.
Yan WL; Guan XY; Green ED; Nicolson R; Yap TK; Zhang J; Jacobsen LK; Krasnewich DM; Kumra S; Lenane MC; Gochman P; Damschroder-Williams PJ; Esterling LE; Long RT; Martin BM; Sidransky E; Rapoport JL; Ginns EI
Am J Med Genet; 2000 Dec; 96(6):749-53. PubMed ID: 11121174
[TBL] [Abstract][Full Text] [Related]
16. Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
Wassink TH; Piven J; Vieland VJ; Jenkins L; Frantz R; Bartlett CW; Goedken R; Childress D; Spence MA; Smith M; Sheffield VC
Am J Med Genet B Neuropsychiatr Genet; 2005 Jul; 136B(1):36-44. PubMed ID: 15892143
[TBL] [Abstract][Full Text] [Related]
17. Delineation and physical separation of novel translocation breakpoints on chromosome 1p in two genetically closely associated childhood tumors.
Steenman MJ; Zijlstra N; Kruitbosch DL; Wiesmeijer C; Larizza L; Voûte PA; Westerveld A; Mannens MM
Cytogenet Cell Genet; 2000; 88(3-4):289-95. PubMed ID: 10828613
[TBL] [Abstract][Full Text] [Related]
18. Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.
Schüle B; Albalwi M; Northrop E; Francis DI; Rowell M; Slater HR; Gardner RJ; Francke U
BMC Med Genet; 2005 May; 6():18. PubMed ID: 15877813
[TBL] [Abstract][Full Text] [Related]
19. Physical mapping of nine Xq translocation breakpoints and identification of XPNPEP2 as a premature ovarian failure candidate gene.
Prueitt RL; Ross JL; Zinn AR
Cytogenet Cell Genet; 2000; 89(1-2):44-50. PubMed ID: 10894934
[TBL] [Abstract][Full Text] [Related]
20. Sequencing and analyzing the t(1;7) reciprocal translocation breakpoints associated with a case of childhood-onset schizophrenia/autistic disorder.
Idol JR; Addington AM; Long RT; Rapoport JL; Green ED
J Autism Dev Disord; 2008 Apr; 38(4):668-77. PubMed ID: 17879154
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]