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Results:
1-15
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Results: 15
Authors:
DeWan, AT
Parrado, AR
Matise, TC
Leal, SM
Citation: At. Dewan et al., The map problem: A comparison of genetic and sequence-based physical maps, AM J HU GEN, 70(1), 2002, pp. 101-107
Authors:
Bespalova, IN
Van Camp, G
Bom, SJH
Brown, DJ
Cryns, K
DeWan, AT
Erson, AE
Flothmann, K
Kunst, HPM
Kurnool, P
Sivakumaran, TA
Cremers, CWRJ
Leal, SM
Burmeister, M
Lesperance, MM
Citation: In. Bespalova et al., Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss, HUM MOL GEN, 10(22), 2001, pp. 2501-2508
Authors:
Wille, A
Leal, SM
Citation: A. Wille et Sm. Leal, Novel selection criteria for genome scans of complex traits, GENET EPID, 21, 2001, pp. S800-S804
Authors:
Cigler, T
LaForge, KS
McHugh, PF
Kapadia, SU
Leal, SM
Kreek, MJ
Citation: T. Cigler et al., Novel and previously reported single-nucleotide polymorphisms in the human5-HT(1B)receptor gene: No association with cocaine or alcohol abuse or dependence, AM J MED G, 105(6), 2001, pp. 489-497
Authors:
Leal, SM
Citation: Sm. Leal, Phenotypes and genetic analysis of psychiatric and neuropsychiatric traits, AM J MED G, 105(1), 2001, pp. 4-7
Authors:
Hu, FZ
Preston, RA
Post, JC
White, GJ
Kikuchi, LW
Wang, X
Leal, SM
Levenstien, MA
Ott, J
Self, TW
Allen, G
Stiffler, RS
McGraw, C
Pulsifer-Anderson, EA
Ehrlich, GD
Citation: Fz. Hu et al., Mapping of a gene for severe pediatric gastroesophageal reflux to chromosome 13q14, J AM MED A, 284(3), 2000, pp. 325-334
Authors:
Salam, AA
Hafner, FM
Linder, TE
Spillmann, T
Schinzel, AA
Leal, SM
Citation: Aa. Salam et al., A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic heaving loss maps to 14q21-q22 in a Swiss German kindred, AM J HU GEN, 66(6), 2000, pp. 1984-1988
Authors:
Hafner, FM
Salam, AA
Linder, TE
Balmer, D
Baumer, A
Schinzel, AA
Spillmann, T
Leal, SM
Citation: Fm. Hafner et al., A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred, AM J HU GEN, 66(4), 2000, pp. 1437-1442
Authors:
Leal, SM
Ott, J
Citation: Sm. Leal et J. Ott, Effects of stratification in the analysis of affected-sib-pair data: Benefits and costs, AM J HU GEN, 66(2), 2000, pp. 567-575
Authors:
Leal, SM
Speer, MC
Citation: Sm. Leal et Mc. Speer, Genetic linkage analysis in human disease, GENETICS OF OSTEOPOROSIS AND METABOLIC BONE DISEASE, 2000, pp. 377-413
Authors:
Leal, SM
Heath, SC
Citation: Sm. Leal et Sc. Heath, Searching for alcoholism susceptibility genes using Markov chain Monte Carlo methods, GENET EPID, 17, 1999, pp. S217-S222
Authors:
Chung, WK
Luke, A
Cooper, RS
Rotini, C
Vidal-Puig, A
Rosenbaum, M
Gordon, D
Leal, SM
Caprio, S
Goldsmith, R
Andreu, AL
Bruno, C
DiMauro, S
Heo, M
Lowe, WL
Lowell, BB
Allison, DB
Leibel, RL
Citation: Wk. Chung et al., The long isoform uncoupling protein-3 (UCP3L) in human energy homeostasis, INT J OBES, 23, 1999, pp. S49-S50
Authors:
Leal, SM
Huang, SS
Huang, JS
Citation: Sm. Leal et al., Interactions of high affinity insulin-like growth factor-binding proteins with the type V transforming growth factor-P receptor in mink lung epithelial cells, J BIOL CHEM, 274(10), 1999, pp. 6711-6717
Authors:
Chung, WK
Luke, A
Cooper, RS
Rotini, C
Vidal-Puig, A
Rosenbaum, M
Chua, M
Solanes, G
Zheng, M
Zhao, L
LeDuc, C
Eisberg, A
Chu, F
Murphy, E
Schreier, M
Aronne, L
Caprio, S
Kahle, B
Gordon, D
Leal, SM
Goldsmith, R
Andreu, AL
Bruno, C
DiMauro, S
Heo, MS
Lowe, WL
Lowell, BB
Allison, DB
Leibel, RL
Citation: Wk. Chung et al., Genetic and physiologic analysis of the role of uncoupling protein 3 in human energy homeostasis, DIABETES, 48(9), 1999, pp. 1890-1895
Authors:
Winick, JD
Blundell, ML
Galke, BL
Salam, AA
Leal, SM
Karayiorgou, M
Citation: Jd. Winick et al., Homozygosity mapping of the achromatopsia locus in the pingelapese, AM J HU GEN, 64(6), 1999, pp. 1679-1685
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