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Science (New York, N.Y.)|September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degenerationR Allikmets, N F Shroyer, N Singh, et al.Human Mutation|October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence changeK T Hiriyanna, E L Bingham, B M Yashar, et al.Genetic Epidemiology|December 19, 2000
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancerG E Airewele, A J Sigurdson, K J Wiley, et al.Human Genetics|February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaM T Bassi, A A Bergen, P Bitoun, et al.Physics in Medicine and Biology|October 21, 2005
Dynamic imaging of the lungs using x-ray phase contrastR A Lewis, N Yagi, M J Kitchen, et al.American Journal of Human Genetics|April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1I Stoilov, A N Akarsu, I Alozie, et al.Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.The British Journal of Radiology|May 24, 2003
X-ray refraction effects: application to the imaging of biological tissuesR A Lewis, C J Hall, A P Hufton, et al.The British Journal of Radiology|October 27, 2005
Phase contrast X-ray imaging of mice and rabbit lungs: a comparative studyM J Kitchen, R A Lewis, N Yagi, et al.Journal of Medical Genetics|October 3, 2009
Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mappingH M Harville, S Held, A Diaz-Font, et al.Pageof 41