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Eye (London, England)|November 27, 2010
Reproducibility and agreement in evaluating retinal nerve fibre layer thickness between Stratus and Spectralis OCTS N Arthur, S D Smith, M M Wright, et al.
American Journal of Human Genetics|June 13, 1998
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing lossP M Kelley, D J Harris, B C Comer, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1988
Homozygous deletion of the alpha- and beta 1-interferon genes in human leukemia and derived cell linesM O Diaz, S Ziemin, M M Le Beau, et al.
Cancer Genetics and Cytogenetics|January 1, 1990
Characterization of the breakpoint of a t(14;14)(q11.2;q32) from the leukemic cells of a patient with T-cell acute lymphoblastic leukemiaV L Bertness, C A Felix, O W McBride, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 1, 1997
A long-term dose-response study of mitomycin in glaucoma filtration surgeryA L Robin, R Ramakrishnan, R Krishnadas, et al.
Kidney International|December 1, 1996
Nitric oxide synthase induction with renal transplant rejection or infectionS D Smith, M A Wheeler, R Zhang, et al.
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