Gardner syndrome in a man with an interstitial deletion of 5q.
about
Attenuated APC alleles produce functional protein from internal translation initiation.Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramificationspp60c-src activation in human colon carcinomaPhenotypic, cytogenetic, and molecular studies of three patients with constitutional deletions of chromosome 5 in the region of the gene for familial adenomatous polyposisUnderstanding phenotypic variation in rodent models with germline Apc mutationsThe ninth Gordon Hamilton-Fairley memorial lecture. Hereditary cancers: clues to mechanisms of carcinogenesis.Mendelian cytogenetics. Chromosome rearrangements associated with mendelian disordersYeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region.An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generationsTwo cases of 5q deletions in patients with familial adenomatous polyposis: possible link with Caroli's disease.A constitutional 5q23 deletion.Adenomatous polyposis coli and a cytogenetic deletion of chromosome 5 resulting from a maternal intrachromosomal insertion.Congenital anomalies and genetic disorders in families of children with central nervous system tumours.Presymptomatic diagnosis in Portuguese FAP families using intragenic RFLPs and (CA)n flanking markers by fluorescence based semiautomated DNA analysis.Germline Missense Changes in the APC Gene and Their Relationship to DiseaseDeletion of band 5q21 in association with a de novo translocation involving 2p and 5q.Genotype to phenotype: analyzing the effects of inherited mutations in colorectal cancer families.Complete deletion of Apc results in severe polyposis in mice.Risk estimation in familial adenomatous polyposis using DNA probes linked to the familial adenomatous polyposis gene.Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes.Adenomatous polyposis coli protein deletion leads to cognitive and autism-like disabilities.Constitutional cytogenetic analysis in men with hereditary testicular germ cell tumor: no evidence of disease-related abnormalities.Mutational analysis of patients with adenomatous polyposis: identical inactivating mutations in unrelated individuals.A genetic study of Gardner syndrome and congenital hypertrophy of the retinal pigment epithelium.Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5Familial adenomatous polyposis: more evidence for disease diversity and genetic heterogeneityCpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.Colonic aberrant crypts in azoxymethane-treated F344 rats have decreased hexosaminidase activity.Two types of putative preneoplastic lesions identified by hexosaminidase activity in whole-mounts of colons from F344 rats treated with carcinogenRearrangement of chromosome 1p in breast cancer correlates with poor prognostic featuresPreimplantation genetic diagnosis of inherited cancer: familial adenomatous polyposis coli.Identification of disease genes by whole genome CGH arrays.From gene mutations to tumours--stem cells in gastrointestinal carcinogenesis.A novel pathogenic germline mutation in the adenomatous polyposis coli gene in a Chinese family with familial adenomatous coli.Risk and surveillance of individuals with heritable factors for colorectal cancer. WHO Collaborating Centre for the Prevention of Colorectal Cancer.More than two decades of Apc modeling in rodentsFamilial and genetic risk of transitional cell carcinoma of the urinary tract.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.The intestinal microbiota, gastrointestinal environment and colorectal cancer: a putative role for probiotics in prevention of colorectal cancer?
P2860
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P2860
Gardner syndrome in a man with an interstitial deletion of 5q.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh-hant
name
Gardner syndrome in a man with an interstitial deletion of 5q.
@en
Gardner syndrome in a man with an interstitial deletion of 5q.
@nl
type
label
Gardner syndrome in a man with an interstitial deletion of 5q.
@en
Gardner syndrome in a man with an interstitial deletion of 5q.
@nl
prefLabel
Gardner syndrome in a man with an interstitial deletion of 5q.
@en
Gardner syndrome in a man with an interstitial deletion of 5q.
@nl
P2093
P356
P1476
Gardner syndrome in a man with an interstitial deletion of 5q.
@en
P2093
P304
P356
10.1002/AJMG.1320250309
P577
1986-11-01T00:00:00Z