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Archives 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-SforzaAmerican Journal of Human Genetics|May 1, 1989
The probability of detecting the origin of nondisjunction of autosomal trisomiesA ChakravartiCurrent Protocols in Human Genetics|April 23, 2008
Statistical analysis of radiation hybrid dataA ChakravartiJournal 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.Genomics|September 1, 1991
A graphical representation of genetic and physical maps: the Marey mapA ChakravartiAmerican Journal of Human Genetics|July 1, 1983
Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibriumA ChakravartiPageof 27