A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

Nanda A. Singh, Carole Charlier, Dora Stauffer, +13

Nature Genetics

ChannelopathiesMolecular NeuroscienceHyperpolarization (Biology)NeurophysiologyGenetics +10

The Gene for Familial Polyposis Coli Maps to the Long Arm of Chromosome 5

M. Leppert, M. Dobbs, Peter Scambler, +11

Science

GeneticsMolecular BiologyPathologyGene CharacterizationMolecular Genetics +17

Benign familial neonatal convulsions linked to genetic markers on chromosome 20

Mark Leppert, Vernon Anderson, T G Quattlebaum, +5

Nature

Mendelian DisorderCytogeneticsGenetic DisorderGeneticsGenetic Epidemiology +4

Linkage of a variant or attenuated form of adenomatous polyposis coli to the adenomatous polyposis coli (APC) locus.

Lisa Spirio, Brith Otterud, Dora Stauffer, +7

PubMed

Mapping recessive ophthalmic diseases: Linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q

Richard A. Lewis, Brith Otterud, Dora Stauffer, +2

Genomics

Chromosome 1QMendelian DisorderGenetic DisorderGeneticsLinkage Analysis +7

Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy

Kevin M. Flanigan, Christin M Coffeen, Lee Sexton, +3

Neuromuscular Disorders

BiologySignificant UtahGenetic DisorderMedicineGenetics +9

Apolipoprotein polymorphisms fail to define risk of coronary artery disease. Results of a prospective, angiographically controlled study.

Hiram W. Marshall, Linda Morrison, Lily Wu, +6

Circulation

Etiological heterogeneity in X-linked spastic paraplegia.

Laura Davis Keppen, Mark Leppert, Peter O'Connell, +5

PubMed

Discordance of T‐cell receptor β‐chain genes in familial multiple sclerosis

Sharon Lynch, John Rose, Jack H. Petajan, +3

Annals of Neurology

Genetic mapping of adrenergic receptor genes in humans

M.R. Hoehe, Brith Otterud, Wen‐Tsong Hsieh, +8

Journal of Molecular Medicine

Adrenal GlandMolecular PhysiologyGeneticsPhysiologyHuman Polymorphism +3