Detalhe da pesquisa
1.
A 1p31.3 deletion encompassing the nuclear factor 1A gene presenting as possible temporal lobe epilepsy in association with schizoaffective disorder.
Neurocase
; 28(4): 382-387, 2022 08.
Artigo
Inglês
| MEDLINE | ID: mdl-36209511
2.
Aggressive B-cell lymphoma with t(3;8)(q27;q24) in an elderly patient.
Am J Hematol
; 97(7): 986-988, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34870872
3.
Influence of clone and deletion size on outcome in chronic lymphocytic leukemia patients with an isolated deletion 13q in a population-based analysis in British Columbia, Canada.
Genes Chromosomes Cancer
; 55(1): 16-24, 2016 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-26391112
4.
Unusual presentation of Burkitt-like lymphoma with 11q aberration in an elderly patient.
Blood
; 133(4): 381, 2019 01 24.
Artigo
Inglês
| MEDLINE | ID: mdl-30679236
5.
Impact of age and treatment institution type on outcomes of patients treated for chronic lymphocytic leukemia in British Columbia, Canada.
Leuk Res
; 103: 106538, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33647819
6.
Comparison of real-world treatment patterns in chronic lymphocytic leukemia management before and after availability of ibrutinib in the province of British Columbia, Canada.
Leuk Res
; 91: 106335, 2020 04.
Artigo
Inglês
| MEDLINE | ID: mdl-32114372
7.
Chronic Lymphocytic Leukemia Patients With Deletion 11q Have a Short Time to Requirement of First-Line Therapy, But Long Overall Survival: Results of a Population-Based Cohort in British Columbia, Canada.
Clin Lymphoma Myeloma Leuk
; 17(6): 382-389, 2017 06.
Artigo
Inglês
| MEDLINE | ID: mdl-28559149
8.
Characterization of treatment and outcomes in a population-based cohort of patients with chronic lymphocytic leukemia referred for cytogenetic testing in British Columbia, Canada.
Leuk Res
; 55: 79-90, 2017 04.
Artigo
Inglês
| MEDLINE | ID: mdl-28157628
9.
Clonal evolution as detected by interphase fluorescence in situ hybridization is associated with worse overall survival in a population-based analysis of patients with chronic lymphocytic leukemia in British Columbia, Canada.
Cancer Genet
; 210: 1-8, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-28212806
10.
Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2.
Eur J Hum Genet
; 22(4): 458-63, 2014 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-24045839
11.
Population-based characterization of the genetic landscape of chronic lymphocytic leukemia patients referred for cytogenetic testing in British Columbia, Canada: the role of provincial laboratory standardization.
Cancer Genet
; 207(7-8): 316-25, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-25441686
12.
Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Eur J Med Genet
; 56(8): 420-5, 2013 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-23727450
13.
Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.
J Autism Dev Disord
; 42(7): 1459-69, 2012 Jul.
Artigo
Inglês
| MEDLINE | ID: mdl-22048961
14.
Understanding the impact of 1q21.1 copy number variant.
Orphanet J Rare Dis
; 6: 54, 2011 Aug 08.
Artigo
Inglês
| MEDLINE | ID: mdl-21824431
15.
A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
Psychiatr Genet
; 18(3): 101-9, 2008 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-18496206
16.
Prenatal cytogenetic assessment and inv(2)(p11.2q13).
Prenat Diagn
; 26(9): 810-3, 2006 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-16821252