74 related articles for article (PubMed ID: 12634868)
1. A candidate region for Asperger syndrome defined by two 17p breakpoints.
Tentler D; Johannesson T; Johansson M; Råstam M; Gillberg C; Orsmark C; Carlsson B; Wahlström J; Dahl N
Eur J Hum Genet; 2003 Feb; 11(2):189-95. PubMed ID: 12634868
[TBL] [Abstract][Full Text] [Related]
2. Analysis of balanced rearrangements of chromosome 6 in acute leukemia: clustered breakpoints in q22-q23 and possible involvement of c-MYB in a new recurrent translocation, t(6;7)(q23;q32 through 36).
Sinclair P; Harrison CJ; Jarosová M; Foroni L
Haematologica; 2005 May; 90(5):602-11. PubMed ID: 15921375
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
5. Analysis of two translocation breakpoints and identification of a negative regulatory element in patients with Rieger's syndrome.
Trembath DG; Semina EV; Jones DH; Patil SR; Qian Q; Amendt BA; Russo AF; Murray JC
Birth Defects Res A Clin Mol Teratol; 2004 Feb; 70(2):82-91. PubMed ID: 14991915
[TBL] [Abstract][Full Text] [Related]
6. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
Mignon-Ravix C; Depetris D; Luciani JJ; Cuoco C; Krajewska-Walasek M; Missirian C; Collignon P; Delobel B; Croquette MF; Moncla A; Kroisel PM; Mattei MG
Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
[TBL] [Abstract][Full Text] [Related]
7. Characterization of a de novo balanced translocation in a patient with moderate mental retardation and dysmorphic features.
Haddad MR; Mignon-Ravix C; Cacciagli P; Mégarbané A; Villard L
Eur J Med Genet; 2009; 52(4):211-7. PubMed ID: 19379847
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individuals.
Baptista J; Prigmore E; Gribble SM; Jacobs PA; Carter NP; Crolla JA
Eur J Hum Genet; 2005 Nov; 13(11):1205-12. PubMed ID: 16118644
[TBL] [Abstract][Full Text] [Related]
9. Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.
Salaverria I; Espinet B; Carrió A; Costa D; Astier L; Slotta-Huspenina J; Quintanilla-Martinez L; Fend F; Solé F; Colomer D; Serrano S; Miró R; Beà S; Campo E
Genes Chromosomes Cancer; 2008 Dec; 47(12):1086-97. PubMed ID: 18709664
[TBL] [Abstract][Full Text] [Related]
10. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular cytogenetic detection of 9q34 breakpoints associated with nail patella syndrome.
Silahtaroglu A; Hol FA; Jensen PK; Erdel M; Duba HC; Geurds MP; Knoers NV; Mariman EC; Tümer Z; Utermann G; Wirth J; Bugge M; Tommerup N
Eur J Hum Genet; 1999 Jan; 7(1):68-76. PubMed ID: 10094193
[TBL] [Abstract][Full Text] [Related]
13. Molecular and transcriptional characterization of 17p loss in B-cell chronic lymphocytic leukemia.
Fabris S; Mosca L; Todoerti K; Cutrona G; Lionetti M; Intini D; Matis S; Colombo M; Agnelli L; Gentile M; Spriano M; Callea V; Festini G; Molica S; Lambertenghi Deliliers G; Morabito F; Ferrarini M; Neri A
Genes Chromosomes Cancer; 2008 Sep; 47(9):781-93. PubMed ID: 18521849
[TBL] [Abstract][Full Text] [Related]
14. Using BAC clones to characterize unbalanced chromosome abnormalities in interphase cells.
Plastira K; Maher E; Fantes J; Ramsay J; Angelopoulou R
Eur J Med Genet; 2006; 49(3):235-46. PubMed ID: 16762825
[TBL] [Abstract][Full Text] [Related]
15. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
16. Identification of a recurrent t(4;6) chromosomal translocation in prostate cancer.
Lane TM; Strefford JC; Yáñez-Muñoz RJ; Purkis P; Forsythe E; Nia T; Hines J; Lu YJ; Oliver RT
J Urol; 2007 May; 177(5):1907-12. PubMed ID: 17437846
[TBL] [Abstract][Full Text] [Related]
17. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes.
Gribble SM; Prigmore E; Burford DC; Porter KM; Ng BL; Douglas EJ; Fiegler H; Carr P; Kalaitzopoulos D; Clegg S; Sandstrom R; Temple IK; Youings SA; Thomas NS; Dennis NR; Jacobs PA; Crolla JA; Carter NP
J Med Genet; 2005 Jan; 42(1):8-16. PubMed ID: 15635069
[TBL] [Abstract][Full Text] [Related]
18. Interphase fluorescence in situ hybridization in multiple myeloma and monoclonal gammopathy of undetermined significance without and with positive plasma cell identification: analysis of 192 cases from the Region of Southern Denmark.
Christensen JH; Abildgaard N; Plesner T; Nibe A; Nielsen O; Sørensen AG; Kerndrup GB;
Cancer Genet Cytogenet; 2007 Apr; 174(2):89-99. PubMed ID: 17452249
[TBL] [Abstract][Full Text] [Related]
19. A cluster of translocation breakpoints in 2q37 is associated with overexpression of NPPC in patients with a similar overgrowth phenotype.
Moncla A; Missirian C; Cacciagli P; Balzamo E; Legeai-Mallet L; Jouve JL; Chabrol B; Le Merrer M; Plessis G; Villard L; Philip N
Hum Mutat; 2007 Dec; 28(12):1183-8. PubMed ID: 17676597
[TBL] [Abstract][Full Text] [Related]
20. Three autosomal chromosome translocations associated with repeated early embryonic loss (REEL) in the domestic horse (Equus caballus).
Lear TL; Lundquist J; Zent WW; Fishback WD; Clark A
Cytogenet Genome Res; 2008; 120(1-2):117-22. PubMed ID: 18467834
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]