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Human Heredity|January 1, 1985
Glutamate pyruvate transaminase null allele (GPT0) in the NavajoM Crist, J R Heckenlively, L L Field, et al.Human Heredity|January 1, 1985
Genetic linkage analysis of the carpal tunnel syndromeR S Sparkes, M A Spence, N L Gottlieb, et al.Human Heredity|January 1, 1984
Genetic linkage studies of transferrin, pseudocholinesterase, and chromosome 1 lociR S Sparkes, L L Field, M C Sparkes, et al.Molecular Psychiatry|July 30, 2008
Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR)L J Strug, R Suresh, A J Fyer, et al.Human Genetics|September 1, 1989
Mapping studies of the serum cholinesterase-2 locus (CHE2)M L Marazita, B J Keats, M A Spence, et al.Neurology|June 1, 1987
The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigreeR M Boustany, E Fleischnick, C A Alper, et al.American Journal of Human Genetics|July 1, 1977
Probable genetic linkage between autosomal dominant retinitis pigmentosa (RP) and amylase (AMY2): evidence of an RP locus on chromosome 1M A Spence, R S Sparkes, J R Heckenlively, et al.Psychiatric Genetics|May 21, 1999
Lack of genetic linkage or association between a functional serotonin transporter polymorphism and panic disorderS P Hamilton, G A Heiman, F Haghighi, et al.American Journal of Human Genetics|June 1, 1986
Cowden disease: gene marker studies and measurements of epidermal growth factorH E Carlson, T W Burns, S L Davenport, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Pseudo low penetrance in retinoblastoma. Fortuitous familial aggregation of sporadic cases caused by independently derived mutations in two large pedigreesF L Munier, M X Wang, M A Spence, et al.Pageof 19