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Proceedings of the National Academy of Sciences of the United States of America|September 1, 1987
Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardationR L Nussbaum, J G Lesko, R A Lewis, et al.Nature Genetics|May 1, 1994
Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneousM Leppert, L Baird, K L Anderson, et al.Ophthalmology|November 1, 1985
Brown oculocutaneous albinism. Clinical, ophthalmological, and biochemical characterizationR A King, R A Lewis, D Townsend, et al.Proceedings of the National Academy of Sciences of the United States of America|March 15, 1992
Isolation of a candidate gene for choroideremiaD E Merry, P A Jänne, J E Landers, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|July 1, 1977
Familial foveal retinoschisisR A Lewis, G B Lee, C L Martonyi, et al.Human Molecular Genetics|December 1, 2001
Cosegregation and functional analysis of mutant ABCR (ABCA4) alleles in families that manifest both Stargardt disease and age-related macular degenerationN F Shroyer, R A Lewis, A N Yatsenko, et al.Proceedings of the National Academy of Sciences of the United States of America|August 1, 1982
Generation of leukotriene C4 from a subclass of mast cells differentiated in vitro from mouse bone marrowE Razin, J M Mencia-Huerta, R A Lewis, et al.Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|May 31, 2021
Temperature-dependent terahertz spectroscopy of l-phenylalanineJ L Allen, T J Sanders, R Plathe, et al.Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|October 27, 2022
Terahertz tyrosine modesT J Sanders, J L Allen, R Plathe, et al.The Journal of Hand Surgery|May 1, 1978
The hand in mixed connective tissue diseaseR A Lewis, J P Adams, N L Gerber, et al.Pageof 41