Detalhe da pesquisa
1.
Concurrent detection of targeted copy number variants and mutations using a myeloid malignancy next generation sequencing panel allows comprehensive genetic analysis using a single testing strategy.
Br J Haematol
; 173(1): 49-58, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26728869
2.
Deletion 2q37 syndrome: Cognitive-behavioral trajectories and autistic features related to breakpoint and deletion size.
Am J Med Genet A
; 170(9): 2282-91, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27282419
3.
IGF2BP1: a novel IGH translocation partner in B acute lymphoblastic leukemia.
Cancer Genet
; 207(7-8): 332-4, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25195122
4.
Unknown partner for USP6 and unusual SS18 rearrangement detected by fluorescence in situ hybridization in a solid aneurysmal bone cyst.
Cancer Genet
; 204(4): 195-202, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21536237