Chromosome 9p21 SNPs Associated with Multiple Disease Phenotypes Correlate with ANRIL ExpressionAspirin in the Chemoprevention of Colorectal Neoplasia: An OverviewIsolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndromeClosing time for CATCH22Can resistant starch and/or aspirin prevent the development of colonic neoplasia? The Concerted Action Polyp Prevention (CAPP) 1 StudyFrequency gradients of DHCR7 mutations in patients with Smith-Lemli-Opitz syndrome in Europe: evidence for different origins of common mutationsCelecoxib for the prevention of sporadic colorectal adenomasTherapeutic levels of aspirin and salicylate directly inhibit a model of angiogenesis through a Cox-independent mechanismConotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11The cylindromatosis gene (cyld1) on chromosome 16q may be the only tumour suppressor gene involved in the development of cylindromasFamilial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor geneGenetic mapping of the human homologue (T) of mouse T(Brachyury) and a search for allele association between human T and spina bifidaStructure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutationsIntestinal tumorigenesis in the Apc1638N mouse treated with aspirin and resistant starch for up to 5 monthsFive-year efficacy and safety analysis of the Adenoma Prevention with Celecoxib Trial.Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.Polymorphisms of the DNA repair gene XRCC1 and the frequency of somatic mutations at the glycophorin A locus in newborns.DNA repair gene polymorphisms, pre-natal factors and the frequency of somatic mutations in the glycophorin-A gene among healthy newborns.May spina bifida result from an X-linked defect in a selective abortion mechanism?Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene.A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.DiGeorge syndrome: part of CATCH 22.Genetic heterogeneity in hereditary haemorrhagic telangiectasia.The 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 familiesA male with type I orofaciodigital syndromeGENETICS. The Human Variome ProjectDiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.Familial adenomatous polyposis.Williams syndrome.A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.Duchenne muscular dystrophy in one of monozygotic twin girlsMeckel syndrome: what are the minimum diagnostic criteria?Defects in the determination of left-right asymmetry.The North Cumbria Community Genetics ProjectSmith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.Neuroferritinopathy: a new inborn error of iron metabolismSecond-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnancies.Survey of HNPCC Management Analysis of Responses from 18 International Cancer Centres.Nutrition in cancer prevention.
P50
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0000 0001 2434 974X
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1952-02-06T00:00:00Z