Detalhe da pesquisa
1.
GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants.
BMC Bioinformatics
; 18(1): 19, 2017 Jan 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28061750
2.
Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum.
J Med Genet
; 51(6): 375-87, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24714694
3.
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7.
BMC Genomics
; 15: 537, 2014 Jun 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-24973960
4.
Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome.
Am J Med Genet A
; 152A(7): 1724-9, 2010 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-20578131
5.
Genome-Wide Analysis of Interchromosomal Interaction Probabilities Reveals Chained Translocations and Overrepresentation of Translocation Breakpoints in Genes in a Cutaneous T-Cell Lymphoma Cell Line.
Front Oncol
; 8: 183, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29900125
6.
Inactivation of RUNX3/p46 Promotes Cutaneous T-Cell Lymphoma.
J Invest Dermatol
; 136(11): 2287-2296, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27377697
7.
Genomic loss of the putative tumor suppressor gene E2A in human lymphoma.
J Exp Med
; 208(8): 1585-93, 2011 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21788410
8.
An integrative approach for analyzing the interplay of genetic and epigenetic changes in tumors.
Arch Pathol Lab Med
; 132(10): 1557-61, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18834209