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Results: 1-8 |
Results: 8
Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data
Authors: Bailey-Wilson, JE Sorant, AJM Malley, JD Presciuttini, S Redner, RA Severini, TA Badner, JA Pajevic, S Jufer, R Baffoe-Bonnie, A Kao, L Doan, BQ Goldstein, JL Holmes, TN Behneman, D Mandal, DM Turley, TN Weissbecker, KA O'Neill, J Pugh, EW
Citation: Je. Bailey-wilson et al., Comparison of novel and existing methods for detection of linkage disequilibrium using parent-child trios in the GAW12 genetic isolate simulated data, GENET EPID, 21, 2001, pp. S378-S383
Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers
Authors: Pugh, EW Papanicolaou, GJ Justice, CM Roy-Gagnon, MH Sorant, AJM Kingman, A Wilson, AF
Citation: Ew. Pugh et al., Comparison of variance components, ANOVA and regression of offspring on midparent (ROMP) methods for SNP markers, GENET EPID, 21, 2001, pp. S794-S799
Characterization of idiopathic scoliosis in a clinically well-defined population
Authors: Miller, NH Schwab, DL Sponseller, PD Manolio, TA Pugh, EW Wilson, AP
Citation: Nh. Miller et al., Characterization of idiopathic scoliosis in a clinically well-defined population, CLIN ORTHOP, (392), 2001, pp. 349-357
Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3
Authors: Wang, K Pugh, EW Griffen, S Doheny, KF Mostafa, WZ al-Aboosi, MM el-Shanti, H Gitschier, J
Citation: K. Wang et al., Homozygosity mapping places the acrodermatitis enteropathica gene on chromosomal region 8q24.3, AM J HU GEN, 68(4), 2001, pp. 1055-1060
Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13
Authors: Kelley, MJ Jawien, W Lin, A Hoffmeister, K Pugh, EW Doheny, KF Korczak, JF
Citation: Mj. Kelley et al., Autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly) is linked to chromosome 22q12-13, HUM GENET, 106(5), 2000, pp. 557-564
Long forms of the dopamine receptor (DRD4) gene VNTR are more prevalent insubstance abusers: No interaction with functional alleles of the catechol-o-methyltransferase (COMT) gene
Authors: Vandenbergh, DJ Rodriguez, LA Hivert, E Schiller, JH Villareal, G Pugh, EW Lachman, H Uhl, GR
Citation: Dj. Vandenbergh et al., Long forms of the dopamine receptor (DRD4) gene VNTR are more prevalent insubstance abusers: No interaction with functional alleles of the catechol-o-methyltransferase (COMT) gene, AM J MED G, 96(5), 2000, pp. 678-683
Possible linkage of alcoholism, monoamine oxidase activity and p300 amplitude to markers on chromosome 12q24
Authors: Juo, SHH Pugh, EW Baffoe-Bonnie, A Kingman, A Sorant, AJM Klein, AP O'Neill, J Mathias, RA Wilson, AF Bailey-Wilson, JE
Citation: Shh. Juo et al., Possible linkage of alcoholism, monoamine oxidase activity and p300 amplitude to markers on chromosome 12q24, GENET EPID, 17, 1999, pp. S193-S198
Environmental covariates: Effects on the power of sib-pair linkage methods
Authors: Mandal, DM Sorant, AJM Pugh, EW Marcus, SE Klein, AP Mathias, RA O'Neill, J Temiyakarn, LF Wilson, AF Bailey-Wilson, JE
Citation: Dm. Mandal et al., Environmental covariates: Effects on the power of sib-pair linkage methods, GENET EPID, 17, 1999, pp. S643-S648
Risultati: 1-8 |