Detalhe da pesquisa
1.
Molecular landscape of mature B-cell lymphoproliferative disorders with BCL3-translocation: A Groupe Francophone de Cytogénétique Hématologique (GFCH)/French Innovative Leukemia Organization (FILO) study.
Am J Hematol
; 2024 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38817040
2.
Isolated isochromosomes i(X)(p10) and idic(X)(q13) are associated with myeloid malignancies and dysplastic features.
Am J Hematol
; 94(11): E285-E288, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31379011
3.
Identification of a transforming MYB-GATA1 fusion gene in acute basophilic leukemia: a new entity in male infants.
Blood
; 117(21): 5719-22, 2011 May 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-21474671
4.
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute Leukemia.
Cancers (Basel)
; 15(7)2023 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046792
5.
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination.
Diagnostics (Basel)
; 13(23)2023 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38066817
6.
Optical genome mapping for prenatal diagnosis: A prospective study.
Clin Chim Acta
; 551: 117594, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37832906
7.
NUP98-MLL fusion in human acute myeloblastic leukemia.
Blood
; 116(13): 2332-5, 2010 Sep 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20558618
8.
Functional analysis of the NUP98-CCDC28A fusion protein.
Haematologica
; 97(3): 379-87, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22058212
9.
Proportion of parents agreeing to delay fetal karyotyping until the third trimester of pregnancy in cases with an indication.
Fetal Diagn Ther
; 31(2): 115-21, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22301792
10.
Prenatal diagnosis on chorionic villi using molecular techniques should be performed from mesenchymal core rather than from direct villi.
Prenat Diagn
; 31(11): 1111-2; author reply 1113, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22021008
11.
Analysis of alterations of WFDC1, a new putative tumour suppressor gene, in hepatocellular carcinoma.
Eur J Hum Genet
; 10(4): 239-44, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-12032731
12.
Parallel FISH and immunohistochemical studies of ALK status in 3244 non-small-cell lung cancers reveal major discordances.
J Thorac Oncol
; 9(3): 295-306, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24518086
13.
Array-based comparative genomic hybridization identifies a high frequency of copy number variations in patients with syndromic overgrowth.
Eur J Hum Genet
; 18(2): 227-32, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19844265
14.
MLL insertion with MLL-MLLT3 gene fusion in acute leukemia: case report and review of the literature.
Cancer Genet Cytogenet
; 183(1): 53-9, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18474298
15.
Prognostic and oncogenic relevance of TLX1/HOX11 expression level in T-ALLs.
Blood
; 110(7): 2324-30, 2007 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-17609427