Familial risk of early and late onset cancer

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منابع مشابه

Familial risk of early and late onset cancer: nationwide prospective cohort study OPEN ACCESS

Objective To determine whether familial risk of cancer is limited to early onset cases. Design Nationwide prospective cohort study. Setting Nationwide Swedish Family-Cancer Database. Participants All Swedes born after 1931 and their biological parents, totalling >12.2 million individuals, including >1.1 million cases of first primary cancer. Main outcome measures Familial risks of the concordan...

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Familial risk of early and late onset cancer: nationwide prospective cohort study

OBJECTIVE To determine whether familial risk of cancer is limited to early onset cases. DESIGN Nationwide prospective cohort study. SETTING Nationwide Swedish Family-Cancer Database. PARTICIPANTS All Swedes born after 1931 and their biological parents, totalling >12.2 million individuals, including >1.1 million cases of first primary cancer. MAIN OUTCOME MEASURES Familial risks of the c...

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Familial aggregation of Parkinson disease: a comparative study of early-onset and late-onset disease.

CONTEXT It is unclear whether late-onset Parkinson disease (PD), which is the most typical and most common form of the disease, has a familial component. Evidence for familial aggregation is key to whether research should focus on gene discovery or search for environmental factors. OBJECTIVE To investigate familial aggregation of early-onset and late-onset PD separately. METHODS Using survi...

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Chromosome 8q24 markers: risk of early-onset and familial prostate cancer.

Recent admixture mapping and linkage/association studies have implicated an approximately 1 Mb region on chromosome 8q24 in prostate cancer susceptibility. In a subsequent follow-up investigation, Haiman et al. (Nat Genet 2007;39:638-44) observed significant, independent associations between 7 markers within this region and sporadic prostate cancer risk in a multi-ethnic sample. To clarify the ...

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Familial muscular dystrophy of late onset.

Two related cases of a proximal muscular dystrophy are described with the full postmortem findings in one of them. The strong family history is recorded. The condition was clinically predominant in the proximal limb muscles and showed an autosomal dominant type of inheritance with complete penetrance.

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ژورنال

عنوان ژورنال: The Journal of the Royal College of Physicians of Edinburgh

سال: 2013

ISSN: 1478-2715,2042-8189

DOI: 10.4997/jrcpe.2013.209