Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
about
Familial adenomatous polyposisAge and manifestation related symptoms in familial adenomatous polyposis.2017 update on the relationship between diabetes and colorectal cancer: epidemiology, potential molecular mechanisms and therapeutic implicationsThe UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variations.Mutational spectrum of APC and genotype-phenotype correlations in Greek FAP patients.Single nucleotide polymorphisms of the APC gene and colorectal cancer risk: a case-control study in TaiwanClinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72.Gastrointestinal tract cancers: Genetics, heritability and germ line mutationsFamilial adenomatous polyposis in three generations of a single family: a case study.Calcium and vitamin D. Their potential roles in colon and breast cancer prevention.Hereditary pancreatic cancer: related syndromes and clinical perspective.Genetic predisposition to colorectal cancer: where we stand and future perspectivesAttenuated familial adenomatous polyposis manifests as autosomal dominant late-onset colorectal cancer.Pancreatic ductal adenocarcinoma: risk factors, screening, and early detection.A de novo missense mutation of the FUS gene in a "true" sporadic ALS case.Familial adenomatous polyposis: ileo-anal pouch versus ileo-rectal anastomosis.Genetic components of perinatal morbidity and mortality.Clinical application of genetics in management of colorectal cancer.Colorectal Cancer Incidence Rates in the Louisiana Acadian Parishes Demonstrated to be Among the Highest in the United States.Parental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome.Extra-intestinal manifestations of familial adenomatous polyposisThe genetic basis of familial adenomatous polyposis and its implications for clinical practice and risk management.Spontaneous immortalization of clinically normal colon-derived fibroblasts from a familial adenomatous polyposis patient.Patterns of proliferative activity in the colonic crypt determine crypt stability and rates of somatic evolution.Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9.Educational needs about cancer family history and genetic counseling for cancer risk among frontline healthcare clinicians in New York CityGenetic 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.Prevalence of skin lesions in familial adenomatous polyposis: a marker for presymptomatic diagnosis?Oral manifestations in patients with familial adenomatous polyposis: A systematic review and meta-analysis.Segmental resection with primary anastomosis is not always safe in splenic flexure perforationGardner's syndrome: genetic testing and colonoscopy are indicated in adolescents and young adults with cranial osteomas: a case report.Determining the frequency of de novo germline mutations in DNA mismatch repair genes.Diagnostic Approach to Hereditary Colorectal Cancer Syndromes.The genetic basis of colonic adenomatous polyposis syndromesACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromesEnhanced intestinal tumor multiplicity and grade in vivo after HZE exposure: mouse models for space radiation risk estimatesClinical Utility Gene Card for: Familial adenomatous polyposis (FAP) and attenuated FAP (AFAP)--update 2014.
P2860
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P2860
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
description
1994 nî lūn-bûn
@nan
1994 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@ast
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@en
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@nl
type
label
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@ast
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@en
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@nl
prefLabel
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@ast
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@en
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@nl
P2093
P356
P1433
P1476
Familial adenomatous polyposis (FAP): frequency, penetrance, and mutation rate.
@en
P2093
P304
P356
10.1002/HUMU.1380030206
P577
1994-01-01T00:00:00Z