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Dominant Characteristics of Osteogenesis Imperfecta

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dc.contributor.author Lehman, Brent P.
dc.date.accessioned 2012-03-02T20:33:04Z
dc.date.available 2012-03-02T20:33:04Z
dc.date.issued 2011-05
dc.identifier.uri http://digital.library.wisc.edu/1793/56935
dc.description Color poster with text, graphs, and images. en
dc.description.abstract Osteogenesis imperfecta (OI) has been characterized as both an autosomal dominant and recessive genetic disease. OI is caused by abnormalities in collagen I fibers. In the dominant form of the disease, two genes COL1A1 or COL1A2 can be mutated to form the faulty collagen I fibers. Individuals with these mutations generally experience mild forms of OI. 90% of patients who exhibit the OI phenotype have the dominant form of the disease. en
dc.description.provenance Submitted by Randy Olson (olsonran@uwec.edu) on 2012-03-02T20:33:04Z No. of bitstreams: 2 LehmanSpr11.ppt: 2151424 bytes, checksum: 62efa1836fbad7f12b6414a59a30e8cb (MD5) LehmanSpr11.pdf: 770975 bytes, checksum: 55df7a1f956729cea3cc58c3336ee228 (MD5) en
dc.description.provenance Made available in DSpace on 2012-03-02T20:33:04Z (GMT). No. of bitstreams: 2 LehmanSpr11.ppt: 2151424 bytes, checksum: 62efa1836fbad7f12b6414a59a30e8cb (MD5) LehmanSpr11.pdf: 770975 bytes, checksum: 55df7a1f956729cea3cc58c3336ee228 (MD5) Previous issue date: 2011-05 en
dc.description.sponsorship University of Wisconsin--Eau Claire Office of Research and Sponsored Programs en
dc.language.iso en_US en
dc.relation.ispartofseries USGZE AS589 en
dc.subject Posters en
dc.subject Osteogenesis imperfecta en
dc.title Dominant Characteristics of Osteogenesis Imperfecta en
dc.type Presentation en

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