172 related articles for article (PubMed ID: 18253027)
1. Intragenic breakpoints localized by array CGH in a t(2;6) familial translocation.
Bernheim A; Toujani S; Guillaud-Bataille M; Richon C; Waxin H; Dessen P; Berger R
Cytogenet Genome Res; 2007; 119(3-4):185-90. PubMed ID: 18253027
[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. Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.
Selzer RR; Richmond TA; Pofahl NJ; Green RD; Eis PS; Nair P; Brothman AR; Stallings RL
Genes Chromosomes Cancer; 2005 Nov; 44(3):305-19. PubMed ID: 16075461
[TBL] [Abstract][Full Text] [Related]
4. Genomic signatures of chromosomal instability and osteosarcoma progression detected by high resolution array CGH and interphase FISH.
Selvarajah S; Yoshimoto M; Ludkovski O; Park PC; Bayani J; Thorner P; Maire G; Squire JA; Zielenska M
Cytogenet Genome Res; 2008; 122(1):5-15. PubMed ID: 18931480
[TBL] [Abstract][Full Text] [Related]
5. Disruption of sodium bicarbonate transporter SLC4A10 in a patient with complex partial epilepsy and mental retardation.
Gurnett CA; Veile R; Zempel J; Blackburn L; Lovett M; Bowcock A
Arch Neurol; 2008 Apr; 65(4):550-3. PubMed ID: 18413482
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Overexpression of the C-type natriuretic peptide (CNP) is associated with overgrowth and bone anomalies in an individual with balanced t(2;7) translocation.
Bocciardi R; Giorda R; Buttgereit J; Gimelli S; Divizia MT; Beri S; Garofalo S; Tavella S; Lerone M; Zuffardi O; Bader M; Ravazzolo R; Gimelli G
Hum Mutat; 2007 Jul; 28(7):724-31. PubMed ID: 17373680
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Translocations involving 6p22 in acute myeloid leukaemia at relapse: breakpoint characterization using microarray-based comparative genomic hybridization.
Tchinda J; Dijkhuizen T; Vlies Pv Pv; Kok K; Horst J
Br J Haematol; 2004 Aug; 126(4):495-500. PubMed ID: 15287941
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular characterization of the t(3;9) associated with immortalization in the MCF10A cell line.
Cowell JK; LaDuca J; Rossi MR; Burkhardt T; Nowak NJ; Matsui S
Cancer Genet Cytogenet; 2005 Nov; 163(1):23-9. PubMed ID: 16271952
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of a 9q34.3 microdeletion by array-CGH in a fetus with an apparently balanced translocation.
Simovich MJ; Yatsenko SA; Kang SH; Cheung SW; Dudek ME; Pursley A; Ward PA; Patel A; Lupski JR
Prenat Diagn; 2007 Dec; 27(12):1112-7. PubMed ID: 17849500
[TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma.
Lastowska M; Van Roy N; Bown N; Speleman F; Roberts P; Lunec J; Strachan T; Pearson AD; Jackson MS
Med Pediatr Oncol; 2001 Jan; 36(1):20-3. PubMed ID: 11464884
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Liehr T; Stumm M; Wegner RD; Bhatt S; Hickmann P; Patsalis PC; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai WW; Cheung SW; Weise A
Cytogenet Genome Res; 2009; 124(1):102-5. PubMed ID: 19372675
[TBL] [Abstract][Full Text] [Related]
17. Identification of cryptic imbalance in phenotypically normal and abnormal translocation carriers.
Gajecka M; Glotzbach CD; Jarmuz M; Ballif BC; Shaffer LG
Eur J Hum Genet; 2006 Dec; 14(12):1255-62. PubMed ID: 16941016
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization].
Zhu G; Bartsch O; Wan M; Gillessen-Kaesbach G; Passarge E
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Apr; 18(2):96-9. PubMed ID: 11295125
[TBL] [Abstract][Full Text] [Related]
20. A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of a t(4;22).
Nimmakayalu MA; Gotter AL; Shaikh TH; Emanuel BS
Hum Mol Genet; 2003 Nov; 12(21):2817-25. PubMed ID: 12952865
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]