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Recessive mutations in the gene encoding the tight junction protein occludin cause band-like calcification with simplified gyration and polymicrogyria.
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria.
Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA.
Deficiency of chromosome 8p21.1----8pter: case report and review of the literature.
Screening initiation with FIT or colonoscopy: Post-hoc analysis of a pragmatic, randomized trial.
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Screening initiation with FIT or colonoscopy: Post-hoc analysis of a pragmatic, randomized trial.
Screening initiation with FIT or colonoscopy: Post-hoc analysis of a pragmatic, randomized trial. Prev Med. 2019 01; 118:332-335.
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PubMed
subject areas
Colonoscopy
Colorectal Neoplasms
Early Detection of Cancer
Female
Health Promotion
Humans
Male
Middle Aged
Occult Blood
Primary Health Care
Randomized Controlled Trials as Topic
authors with profiles
Caitlin Murphy