Showing results (21-30 of 117) with videos related to
Sort By:
Pageof 12
Genetica|August 31, 1987
Evolution of nuclear gene families in primates. Copy-number variation in the argininosuccinate synthetase (ASS) pseudogene family and the anonymous DNA sequence, D1S1S P Daiger, M E Goode, B D TrowbridgeArchives of Ophthalmology (Chicago, Ill. : 1960)|January 1, 1991
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsinJ R Heckenlively, J A Rodriguez, S P DaigerAnnals of Human Genetics|January 1, 1992
Apparent heterozygote deficiencies observed in DNA typing data and their implications in forensic applicationsR Chakraborty, M De Andrade, S P Daiger, et al.American Journal of Human Genetics|November 1, 1977
Detection of genetic variation with radioactive ligands. I. Electrophoretic screening of plasma proteins with a selected panel of compoundsL L Cavalli-Sforza, S P Daiger, D P RummelProceedings of the National Academy of Sciences of the United States of America|June 1, 1975
Group-specific component (Gc) proteins bind vitamin D and 25-hydroxyvitamin DS P Daiger, M S Schanfield, L L Cavalli-SforzaJournal of Medical Genetics|June 1, 1997
Molecular analysis of the human vitamin D binding protein (group specific component, Gc) in tuberous sclerosis complex (TSC)J A Rodriguez, R L Evans, S P Daiger, et al.Molecular Vision|May 6, 1999
Identifying and mapping novel retinal-expressed ESTs from humansK Malone, M M Sohocki, L S Sullivan, et al.American Journal of Human Genetics|April 1, 1986
The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1M E Goode, P vanTuinen, D H Ledbetter, et al.American Journal of Ophthalmology|November 13, 2001
Splice site mutation in the peripherin/RDS gene associated with pattern dystrophy of the retinaJ E Sears, T A Aaberg, S P Daiger, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 23, 2001
Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humansM M Sohocki, L S Sullivan, D L Tirpak, et al.Pageof 12