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The American Journal of Psychiatry|February 1, 1988
Electroretinograms in autism: a pilot study of b-wave amplitudesE R Ritvo, D Creel, G Realmuto, et al.Investigative Ophthalmology & Visual Science|August 11, 2000
A new locus for autosomal dominant cataract on chromosome 12q13J B Bateman, M Johannes, P Flodman, et al.Genomics|September 15, 1994
Assignment of the zeta-crystallin gene (CRYZ) to human chromosome 1p22-p31 and identification of restriction fragment length polymorphismsC Heinzmann, T L Kojis, P Gonzalez, et al.Somatic Cell and Molecular Genetics|September 1, 1984
Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin geneJ H Fisher, Y E Miller, R S Sparkes, et al.Ophthalmic Genetics|October 18, 2000
Mutational analysis and clinical correlation in Leber congenital amaurosisS R Dharmaraj, E R Silva, A L Pina, et al.Transactions of the American Ophthalmological Society|January 1, 1993
Linkage analysis of Norrie disease with an X-chromosomal ornithine aminotransferase locusJ B Bateman, T L Kojis, R M Cantor, et al.Human Heredity|January 1, 1984
Estimating the recombination frequency for the MN and the Ss lociM A Spence, L L Field, M L Marazita, et al.American Journal of Human Genetics|August 3, 2001
Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophyS E Wilkie, Y Li, E C Deery, et al.Pageof 17