Detalhe da pesquisa
1.
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer.
Nat Genet
; 30(4): 406-10, 2002 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11865300
2.
Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.
Clin Cancer Res
; 12(10): 3209-15, 2006 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16707622
3.
Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome.
BMC Genomics
; 6: 38, 2005 Mar 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-15774015
4.
Contribution of germline mutations in BRCA2, P16(INK4A), P14(ARF) and P15 to uveal melanoma.
Invest Ophthalmol Vis Sci
; 44(2): 458-62, 2003 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-12556369
5.
Mapping of a translocation breakpoint in a Peutz-Jeghers hamartoma to the putative PJS locus at 19q13.4 and mutation analysis of candidate genes in polyp and STK11-negative PJS cases.
Genes Chromosomes Cancer
; 41(2): 163-9, 2004 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-15287029