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Genomics|August 22, 2000
Isolation and characterization of a human chromosome 21q22.3 gene (WDR4) and its mouse homologue that code for a WD-repeat proteinJ Michaud, J Kudoh, A Berry, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2000
Jewish and Middle Eastern non-Jewish populations share a common pool of Y-chromosome biallelic haplotypesM F Hammer, A J Redd, E T Wood, et al.
Human Genetics|April 3, 2001
Isolation and characterization of the UBASH3A gene on 21q22.3 encoding a potential nuclear protein with a novel combination of domainsM Wattenhofer, K Shibuya, J Kudoh, et al.
European Journal of Human Genetics : EJHG|January 1, 1993
A Pst+ polymorphism in the HEXA gene with an unusual geographic distributionF Kaplan, S Kapoor, D Lee, et al.
Human Genetics|October 6, 1998
A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locusK K Kidd, B Morar, C M Castiglione, et al.
Genomics|December 9, 2000
Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiencyL Bartoloni, M Wattenhofer, J Kudoh, et al.
Molecular Psychiatry|April 21, 2004
COMT haplotypes suggest P2 promoter region relevance for schizophreniaM A Palmatier, A J Pakstis, W Speed, et al.
Nature Genetics|January 4, 2001
Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafnessH S Scott, J Kudoh, M Wattenhofer, et al.
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