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Neuropediatrics|April 1, 1996
Cobblestone lissencephaly with normal eyes and muscleW B Dobyns, M A Patton, R F Stratton, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 1, 1991
Familial renal adysplasiaB Murugasu, B R Cole, E P Hawkins, et al.Molecular Vision|March 9, 2000
Evaluation of human diacylglycerol kinase(iota), DGKI, a homolog of Drosophila rdgA, in inherited retinopathy mapping to 7qS J Bowne, L S Sullivan, L Ding, et al.Eye (London, England)|November 7, 2009
Long-term follow-up of a family with dominant X-linked retinitis pigmentosaD M Wu, H Khanna, P Atmaca-Sonmez, et al.American Journal of Human Genetics|May 1, 1989
Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and SwitzerlandS E Sullivan, S D Moore, J M Connor, et al.Journal of Medical Genetics|February 11, 1990
Linkage analysis in Marfan syndromeR C Schwartz, S H Blanton, C A Hyde, et al.American Journal of Veterinary Research|January 1, 1997
Linkage of a microsatellite marker to the canine copper toxicosis locus in Bedlington terriersV Yuzbasiyan-Gurkan, S H Blanton, Y Cao, et al.American Journal of Human Genetics|June 1, 1996
Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversionV Shashi, W L Golden, P S Allinson, et al.American Journal of Human Genetics|August 1, 1989
Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU)S P Daiger, L Reed, S S Huang, et al.Cytogenetics and Cell Genetics|January 1, 1989
Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groupsS P Daiger, M M Humphries, N Giesenschlag, et al.Pageof 12