Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5
about
Cytogenetic and molecular delineation of the smallest commonly deleted region of chromosome 5 in malignant myeloid diseasesPhenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposisLoss of constitutional heterozygosity on chromosome 5q in hepatocellular carcinoma without cirrhosis.Genetic and radiation hybrid mapping of the hyperekplexia region on chromosome 5q.An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generationsThe UK Northern region genetic register for familial adenomatous polyposis coli: use of age of onset, congenital hypertrophy of the retinal pigment epithelium, and DNA markers in risk calculations.Linkage analysis in adenomatous polyposis coli: the use of four closely linked DNA probes in 20 UK familiesDiastrophic dysplasia gene maps to the distal long arm of chromosome 5Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim.Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families.Overview of screening and management of familial adenomatous polyposis.Risk estimation in familial adenomatous polyposis using DNA probes linked to the familial adenomatous polyposis gene.Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.Colorectal adenomas and cancer link to chromosome 13q22.1-13q31.3 in a large family with excess colorectal cancer.Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene.A CA-repeat polymorphism close to the adenomatous polyposis coli (APC) gene offers improved diagnostic testing for familial APC.Fine-scale mapping of the gene responsible for multiple endocrine neoplasia type 1 (MEN 1).Genetic and physical mapping on chromosome 4 narrows the localization of the gene for facioscapulohumeral muscular dystrophy (FSHD)Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.High-resolution linkage mapping for susceptibility genes in human polygenic disease: insulin-dependent diabetes mellitus and chromosome 11q.Exclusion of the retinoblastoma gene and chromosome 13q as the site of a primary lesion for human breast cancer.Genetic linkage map of six polymorphic DNA markers around the gene for familial adenomatous polyposis on chromosome 5.Localization of the genetic defect in multiple endocrine neoplasia type 1 within a small region of chromosome 11.Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expressionCpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.Allele loss from 5q21 (APC/MCC) and 18q21 (DCC) and DCC mRNA expression in breast cancer.Congenital hypertrophy of the retinal pigment epithelium and mandibular osteomata as markers in familial colorectal cancerRisk and surveillance of individuals with heritable factors for colorectal cancer. WHO Collaborating Centre for the Prevention of Colorectal Cancer.Extracolonic manifestations associated with familial adenomatous polyposisSuppression of deregulated c-MYC expression in human colon carcinoma cells by chromosome 5 transfer.Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers.Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients.How Far Do We Go With Genetic Evaluation? Gene, Panel, and Tumor Testing.Chromosomal sites for hepatitis B virus integration in human hepatocellular carcinoma.CA repeat polymorphism at the D5S82 locus, proximal to adenomatous polyposis coli (APC).Lipoprotein lipase deficiency resulting from a nonsense mutation in exon 3 of the lipoprotein lipase gene.The genetics of inherited colon cancer.Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblingsEstablishment and characterization of an epithelial cell line with quasi-normal chromosomes from a tubular adenoma of a familial polyposis coli patient.
P2860
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P2860
Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5
description
1988 nî lūn-bûn
@nan
1988 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1988 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
1988年の論文
@ja
1988年論文
@yue
1988年論文
@zh-hant
1988年論文
@zh-hk
1988年論文
@zh-mo
1988年論文
@zh-tw
1988年论文
@wuu
name
Localization of the genetic de ...... a small region of chromosome 5
@ast
Localization of the genetic de ...... a small region of chromosome 5
@en
type
label
Localization of the genetic de ...... a small region of chromosome 5
@ast
Localization of the genetic de ...... a small region of chromosome 5
@en
prefLabel
Localization of the genetic de ...... a small region of chromosome 5
@ast
Localization of the genetic de ...... a small region of chromosome 5
@en
P2093
P2860
P1476
Localization of the genetic de ...... a small region of chromosome 5
@en
P2093
Fujimoto E
Nakamura Y
P2860
P304
P407
P50
P577
1988-11-01T00:00:00Z