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Nature Genetics|January 23, 1999
Population genetics--making sense out of sequenceA Chakravarti
Human Genetics|October 1, 1991
Information content of the Centre d'Etude du Polymorphisme Humain (CEPH) family structures for linkage studiesA Chakravarti
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.
The American Journal of Cardiology|February 1, 1984
Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors?L P ten Kate, H Boman, S P Daiger, et al.
Chinese Medical Journal|June 1, 1992
Linkage between Rh blood group and autosomal dominant retinitis pigmentosa in ten Chinese familiesY J Fei, S H Blanton, S P Daiger, et al.
American Journal of Human Genetics|July 1, 1981
Detection of genetic variation with radioactive ligands. IV. X-linked, polymorphic genetic variation of thyroxin-binding globulin (TBG)S P Daiger, D P Rummel, L Wang, et al.
Progress in Clinical and Biological Research|January 1, 1987
DNA linkage studies of degenerative retinal diseasesS P Daiger, J R Heckenlively, R A Lewis, et al.
Ophthalmic Genetics|August 1, 2000
Visual phenotype in patients with Arg41Gln and ala196+1bp mutations in the CRX geneR T Tzekov, M M Sohocki, S P Daiger, et al.
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