Report of the Second International Workshop on Human Chromosome 3 mapping

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Angiotensin-converting enzyme (ACE) alleles in the Quechua, a high altitude South American native population Ann. Hum. Biol. 26 4 375-80 1999 1774 PU000025H Rupert JL, Devine DV, Hochachka PW. Frequencies of alleles associated with the increased risk of cardiovascular disease in high altitude natives J. Mol. Cell. Cardio. 31 5 A38 1999 281 PU000026I Tishkoff SA, Dietzsch E, Speed W, Pakstis AJ, Cheung K, Kidd JR, Bonne-Tamir B, Santachiara-Benerecetti AS, Moral P, Watson E, Krings M, Paabo S, Risch N, Jenkins T, Kidd KK. Global patterns of linkage disequilibrium at the CD4 locus and modern human origins Science 271 5254 1380-7 1996 249 PU000027J Kidd JR, Pakstis AJ, Zhao H, Lu RB, Okonofua FE, Odunsi A, Grigorenko E, Bonne-Tamir B, Friedlaender J, Shulz LO, Parnas J, Kidd KK. Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus (PAH) in a global representation of populations Am. J. Hum. Genet. 66 1882-1899 2000 5761 PU000028K Wu J, Kidd KK. Extensive sequence polymorphisms associated with chromosome 10 alpha satellite DNA and its close linkage to markers from the pericentromeric region Human Genetics 84 279-82 1990 204 PU000029L Wu J, Carson NL, Myers S, Pakstis AJ, Kidd JR, Castiglione CM, Anderson L, Hoyle LS, Genel M, Simpson NE, Kidd KK. The genetic defect in multiple endocrine neoplasia type 2A maps next to the centromere of chromosome 10 American Journal of Human Genetics 46 3 624-30 1990 281 PU000030D Kidd JR, Matsubara Y, Castiglione CM, Tanaka K, Kidd KK. The locus for the medium-chain acyl-CoA dehydrogenase gene on chromosome 1 is highly polymorphic Genomics 6 89-93 1990 205 PU000031E Pauls DL, Pakstis AJ, Kurlan R, Kidd KK, Leckman JF, Cohen DJ, Kidd JR, Como P, Sparkes R. Segregation and linkage analyses of Gilles de la Tourette's syndrome and related disorders Journal of the American Academy of Child and Adolescent Psychiatry 29 195-203 1990 216 PU000032F Kennedy JL, Giuffra LA, Cavalli-Sforza LL, Pakstis AJ, Kidd JR, Sjogren B, Wetterberg L, Kidd KK. Searching for genes predisposing to neuropsychiatric disorders In: From Phenotype to Gene in Common Disorders (K. Berg, N. Retterstol, S. Refsum, Eds.) 251-64 1990 281 PU000033G White R, Lalouel JM, Nakamura Y, Donis-Keller H, Green P, Bowden D, Mathew C, Easton D, Robson E, Morton N, Gusella J, Haines J, Retief A, Kidd K, Murray J, Lathrop M, Cann H. The CEPH Consortium primary linkage map of human chromosome 10 Genomics 6 393-412 1990 206 PU000034H Wu J, Kidd KK. HincII polymorphism at the D10S95 locus Nucleic Acids Research 18 4965 1990 281 PU000035I Wu J, Kidd KK. High frequency PvuII and PstI polymorphisms identified by KW31 (D10S96) on chromosome 10 Nucleic Acids Research 18 1316 1990 281 PU000036J Wu J, Kidd KK. An EcoRI polymorphism identified by KW6 (D10S97) on chromosome 10 Nucleic Acids Research 18 1316 1990 281 PU000037K Ruano G, Kidd KK, Stephens JC. Haplotype of multiple polymorphisms resolved by enzymatic amplification of single DNA molecules Proceedings of the National Academy of Sciences USA 87 6296-6300 1990 156 PU000038L Ruano G, Gray MR, Miki T, Ferguson-Smith AC, Ruddle FH, Kidd KK. Monomorphism among humans and sequence differences among higher primates for a Sequence Tagged Site (STS) in homeo box cluster 2 Nucleic Acids Research 18 1314 1990 281 PU000039M Gelernter J, Pakstis AJ, Pauls DL, Kurlan R, Gancher ST, Civelli O, Grandy D, Kidd KK. Tourette Syndrome is not linked to Dsub2/sub dopamine receptor Archives of General Psychiatry 47 1073-77 1990 156 PU000040E Simpson NE, Kidd KK. Closing in on the MEN2A locus Henry Ford Hospital Medical Journal 37 100-5 1990 218 PU000041F Kidd KK, Simpson NE. The search for the gene for MEN 2A Recent Advances in Hormone Research 46 305-43 1990 281 PU000042G Kidd KK, Cavalli-Sforza LL, Wetterberg L. A genetic linkage study of schizophrenia In: Proceedings of the VII World Congress of Psychiatry Athens 1990 281 PU0