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Human Genetics|October 18, 2002
Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneityGerald Stöber, Dominik Seelow, Franz Rüschendorf, et al.Human Genetics|October 18, 2002
A detailed physical map of the 6p reading disability locus, including new markers and confirmation of recombination suppressionJung Ahn, Tae-Woong Won, Deborah E Kaplan, et al.Human Genetics|October 18, 2002
A novel mutation in the IHH gene causes brachydactyly type A1: a 95-year-old mystery resolvedM Elizabeth McCready, Elizabeth Sweeney, Allan E Fryer, et al.Human Genetics|October 18, 2002
Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11Leila Baghernajad Salehi, Massimo Mangino, Salvatore De Serio, et al.Human Genetics|October 18, 2002
CTLA-4 gene polymorphisms in systemic lupus erythematosus: a highly significant association with a determinant in the promoter regionLori L Hudson, Keith Rocca, Yeong W Song, et al.Human Genetics|June 16, 1999
The human neuregulin-2 (NRG2) gene: cloning, mapping and evaluation as a candidate for the autosomal recessive form of Charcot-Marie-Tooth disease linked to 5qH Z Ring, H Chang, A Guilbot, et al.Human Genetics|June 16, 1999
The spectrum of microsatellite loci on chromosomes 7 and 8 in Taiwan aboriginal populations: a comparative population genetic studyC C Wei, F T Chiang, K S Lin, et al.Human Genetics|June 16, 1999
Testing the nonrandomness of chromosomal breakpoints using highest observed breakagesC D Hou, J Chiang, J J TaiHuman Genetics|September 10, 1999
NPC1 gene mutations in Japanese patients with Niemann-Pick disease type CT Yamamoto, E Nanba, H Ninomiya, et al.Human Genetics|September 10, 1999
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminomaF von Deimling, J M Scharf, T Liehr, et al.Pageof 959