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Results:
1-13
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Results: 13
Authors:
Liu, JJ
Juo, SH
Holopainen, P
Terwilliger, J
Tong, XM
Grunn, A
Brito, M
Green, P
Mustalahti, K
Maki, M
Gilliam, TC
Partanen, J
Citation: Jj. Liu et al., Genomewide linkage analysis of celiac disease in Finnish families, AM J HU GEN, 70(1), 2002, pp. 51-59
Authors:
Alarcon, M
Cantor, RM
Liu, JJ
Gilliam, TC
Geschwind, DH
Citation: M. Alarcon et al., Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families, AM J HU GEN, 70(1), 2002, pp. 60-71
Authors:
Liu, JJ
Juo, SH
Terwilliger, JD
Grunn, A
Tong, XM
Brito, M
Loth, JE
Kanyas, K
Lerer, B
Endicott, J
Penchaszadeh, G
Gilliam, TC
Baron, M
Citation: Jj. Liu et al., A follow-up linkage study supports evidence for a bipolar affective disorder locus on chromosome 21q22, AM J MED G, 105(2), 2001, pp. 189-194
Authors:
Liu, JJ
Nyholt, DR
Magnussen, P
Parano, E
Pavone, P
Geschwind, D
Lord, C
Iversen, P
Hoh, J
Ott, J
Gilliam, TC
Citation: Jj. Liu et al., A genomewide screen for autism susceptibility loci, AM J HU GEN, 69(2), 2001, pp. 327-340
Authors:
Ranta, S
Zhang, YH
Ross, B
Takkunen, E
Hirvasniemi, A
de la Chapelle, A
Gilliam, TC
Lehesjoki, AE
Citation: S. Ranta et al., Positional cloning and characterisation of the human DLGAP2 gene and its exclusion in progressive epilepsy with mental retardation, EUR J HUM G, 8(5), 2000, pp. 381-384
Authors:
Aita, VM
Ahmad, W
Panteleyev, AA
Kozlowska, U
Kozlowska, A
Gilliam, TC
Jablonska, S
Christiano, AM
Citation: Vm. Aita et al., A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions, EXP DERMATO, 9(2), 2000, pp. 157-162
Authors:
Ranta, S
Zhang, YH
Ross, B
Lonka, L
Takkunen, E
Messer, A
Sharp, J
Wheeler, R
Kusumi, K
Mole, S
Liu, WC
Soares, MB
Bonaldo, MD
Hirvasniemi, A
de la Chapelle, A
Gilliam, TC
Lehesjoki, AE
Citation: S. Ranta et al., The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8, NAT GENET, 23(2), 1999, pp. 233-236
Authors:
Buiakova, OI
Xu, J
Lutsenko, S
Zeitlin, S
Das, K
Das, S
Ross, BM
Mekios, C
Scheinberg, IH
Gilliam, TC
Citation: Oi. Buiakova et al., Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation, HUM MOL GEN, 8(9), 1999, pp. 1665-1671
Authors:
Aita, VM
Christiano, AM
Gilliam, TC
Citation: Vm. Aita et al., Mapping complex traits in diseases of the hair and skin, EXP DERMATO, 8(6), 1999, pp. 439-452
Authors:
Aita, VM
Liang, XH
Murty, VVVS
Pincus, DL
Yu, WP
Cayanis, E
Kalachikov, S
Gilliam, TC
Levine, B
Citation: Vm. Aita et al., Cloning and genomic organization of beclin 1, a candidate tumor suppressorgene on chromosome 17q21, GENOMICS, 59(1), 1999, pp. 59-65
Authors:
Lewis, CA
Batlle, IR
Batlle, KGR
Banerjee, P
Cideciyan, AV
Huang, JC
Aleman, TS
Huang, YJ
Ott, J
Gilliam, TC
Knowles, JA
Jacobson, SG
Citation: Ca. Lewis et al., Tubby-like protein 1 homozygous splice-site mutation causes early-onset severe retinal degeneration, INV OPHTH V, 40(9), 1999, pp. 2106-2114
Authors:
Larin, D
Mekios, C
Das, K
Ross, B
Yang, AS
Gilliam, TC
Citation: D. Larin et al., Characterization of the interaction between the Wilson and Menkes disease proteins and the cytoplasmic copper chaperone, HAH1p, J BIOL CHEM, 274(40), 1999, pp. 28497-28504
Authors:
Aita, VM
Liu, JJ
Knowles, JA
Terwilliger, JD
Baltazar, R
Grunn, A
Loth, JE
Kanyas, K
Lerer, B
Endicott, J
Wang, ZY
Penchaszadeh, G
Gilliam, TC
Baron, M
Citation: Vm. Aita et al., A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus, AM J HU GEN, 64(1), 1999, pp. 210-217
Risultati:
1-13
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