Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene
about
Variable phenotype of familial adenomatous polyposis in pedigrees with 3' mutation in the APC gene.Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.Molecular analysis of the APC and MUTYH genes in Galician and Catalonian FAP families: a different spectrum of mutations?BRCA1 mutations in a selected series of breast/ovarian cancer patients.Clinical application of genetics in management of colorectal cancer.Phenotypic differences in familial adenomatous polyposis based on APC gene mutation status.Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9.Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneityMolecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predispositionDuodenal cancer in patients with familial adenomatous polyposis (FAP): results of a 10 year prospective studyGenetic and clinical characterisation of familial adenomatous polyposis: a population based studyInactivation of promoter 1B of APC causes partial gene silencing: evidence for a significant role of the promoter in regulation and causative of familial adenomatous polyposis.Severe upper gastrointestinal polyposis associated with sparse colonic polyposis in a familial adenomatous polyposis family with an APC mutation at codon 1520.Extra-abdominal desmoid tumors associated with familial adenomatous polyposisContribution of APC and MUTYH mutations to familial adenomatous polyposis susceptibility in HungaryDesmoid tumors: clinical features and outcome of an unpredictable and challenging manifestation of familial adenomatous polyposis.APC gene mutations and extraintestinal phenotype of familial adenomatous polyposis.Recurrent desmoids determine outcome in patients with Gardner syndrome: a cohort study of three generations of an APC mutation-positive family across 30 years.Novel mouse model for Gardner syndrome generated by a large-scale N-ethyl-N-nitrosourea mutagenesis program.Mutation analysis of the APC gene in unrelated Korean patients with FAP: four novel mutations with unusual phenotype.Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene.
P2860
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P2860
Correlation between the development of extracolonic manifestations in FAP patients and mutations beyond codon 1403 in the APC gene
description
1996 nî lūn-bûn
@nan
1996 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1996 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
name
Correlation between the develo ...... ond codon 1403 in the APC gene
@ast
Correlation between the develo ...... ond codon 1403 in the APC gene
@en
type
label
Correlation between the develo ...... ond codon 1403 in the APC gene
@ast
Correlation between the develo ...... ond codon 1403 in the APC gene
@en
prefLabel
Correlation between the develo ...... ond codon 1403 in the APC gene
@ast
Correlation between the develo ...... ond codon 1403 in the APC gene
@en
P2093
P2860
P356
P1476
Correlation between the develo ...... ond codon 1403 in the APC gene
@en
P2093
Guldenschuh I
Hürliman R
P2860
P304
P356
10.1136/JMG.33.4.274
P407
P577
1996-04-01T00:00:00Z