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American Journal of Human Genetics|October 3, 2000
Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolismB S Andresen, E Christensen, T J Corydon, et al.American Journal of Human Genetics|October 3, 2000
General equations for Pt, Ps, and the power of the TDT and the affected-sib-pair testR McGinnisAmerican Journal of Human Genetics|October 3, 2000
Mutations of the SCO1 gene in mitochondrial cytochrome c oxidase deficiency with neonatal-onset hepatic failure and encephalopathyI Valnot, S Osmond, N Gigarel, et al.American Journal of Human Genetics|October 3, 2000
Cloning of the gene encoding a novel integral membrane protein, mucolipidin-and identification of the two major founder mutations causing mucolipidosis type IVM T Bassi, M Manzoni, E Monti, et al.American Journal of Human Genetics|October 7, 2000
A second-generation genomewide screen for asthma-susceptibility alleles in a founder populationC Ober, A Tsalenko, R Parry, et al.American Journal of Human Genetics|September 14, 2000
Significant linkage for Tourette syndrome in a large French Canadian familyC Mérette, A Brassard, A Potvin, et al.American Journal of Human Genetics|September 14, 2000
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13Y A Lee, F Rüschendorf, C Windemuth, et al.American Journal of Human Genetics|June 8, 2000
Comparison of tests for association and linkage in incomplete familiesA C Cervino, A V HillAmerican Journal of Human Genetics|May 29, 2000
A short tandem repeat-based phylogeny for the human Y chromosomeP Forster, A Röhl, P Lünnemann, et al.American Journal of Human Genetics|May 29, 2000
Association mapping in structured populationsJ K Pritchard, M Stephens, N A Rosenberg, et al.Pageof 981