Detalhe da pesquisa
1.
Supporting caregivers of children born prematurely in the development of language: A scoping review.
Paediatr Child Health
; 26(1): e17-e24, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33542775
2.
Familial breast cancer and DNA repair genes: Insights into known and novel susceptibility genes from the GENESIS study, and implications for multigene panel testing.
Int J Cancer
; 144(8): 1962-1974, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30303537
3.
Endoscopic Phenotype of Monoallelic Carriers of MUTYH Gene Mutations in the Family of Polyposis Patients: A Prospective Study.
Dis Colon Rectum
; 62(4): 470-475, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30640315
4.
Haploinsufficiency for NR3C1, the gene encoding the glucocorticoid receptor, in blastic plasmacytoid dendritic cell neoplasms.
Blood
; 127(24): 3040-53, 2016 06 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-27060168
5.
Telomere length, ATM mutation status and cancer risk in Ataxia-Telangiectasia families.
Carcinogenesis
; 38(10): 994-1003, 2017 10 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28981872
6.
A germline mutation in PBRM1 predisposes to renal cell carcinoma.
J Med Genet
; 52(6): 426-30, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25911086
7.
Somatic MMR gene mutations as a cause for MSI-H sebaceous neoplasms in Muir-Torre syndrome-like patients.
Hum Mutat
; 36(3): 292-5, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25504677
8.
Human MSH6 deficiency is associated with impaired antibody maturation.
J Immunol
; 188(4): 2023-9, 2012 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22250089
9.
Telomeric damage in early stage of chronic lymphocytic leukemia correlates with shelterin dysregulation.
Blood
; 118(5): 1316-22, 2011 Aug 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-21355086
10.
Cloned IGH VDJ targets as tools for personalized minimal residual disease monitoring in mature lymphoid malignancies; a feasibility study in mantle cell lymphoma by the Groupe Ouest Est d'Etude des Leucémies et Autres Maladies du Sang.
Br J Haematol
; 158(2): 186-197, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22626453
11.
Accurate detection of the tumor clone in peripheral T-cell lymphoma biopsies by flow cytometric analysis of TCR-Vß repertoire.
Mod Pathol
; 25(9): 1246-57, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22627740
12.
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma.
J Med Genet
; 48(4): 226-34, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21398687
13.
Intensity-dependent constitutional MLH1 promoter methylation leads to early onset of colorectal cancer by affecting both alleles.
Genes Chromosomes Cancer
; 50(3): 178-85, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21213371
14.
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
JAMA
; 305(22): 2304-10, 2011 Jun 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21642682
15.
Identification, characterisation and regulation by CD40 activation of novel CD95 splice variants in CD95-apoptosis-resistant, human, B-cell non-Hodgkin's lymphoma.
Exp Cell Res
; 315(19): 3281-93, 2009 Nov 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19751723
16.
When pictures take away from the message: An examination of young adults' attention to texting and driving advertisements.
Can J Exp Psychol
; 74(2): 131-143, 2020 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-31613130
17.
National recommendations of the French Genetics and Cancer Group - Unicancer on the modalities of multi-genes panel analyses in hereditary predispositions to tumors of the digestive tract.
Eur J Med Genet
; 63(12): 104080, 2020 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-33039684
18.
Osteosarcoma without prior retinoblastoma related to RB1 low-penetrance germline pathogenic variants: A novel type of RB1-related hereditary predisposition syndrome?
Mol Genet Genomic Med
; 7(12): e913, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31568710
19.
The contribution of large genomic deletions at the CDKN2A locus to the burden of familial melanoma.
Br J Cancer
; 99(2): 364-70, 2008 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-18612309
20.
CXCR5 and ICOS expression identifies a CD8 T-cell subset with TFH features in Hodgkin lymphomas.
Blood Adv
; 2(15): 1889-1900, 2018 08 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-30087107