American journal of human genetics

Assessing the feasibility of linkage disequilibrium methods for mapping complex traits: an initial screen for bipolar disorder loci on chromosome 18.

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans.

Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

Mutation and polymorphism of the prion protein gene in Libyan Jews with Creutzfeldt-Jakob disease (CJD).

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

DNA length polymorphism located 5' to the human myelin basic protein gene.

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