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Results: 1-12 |
Results: 12

Authors: Wain, HM White, JA Bruford, E Povey, S
Citation: Hm. Wain et al., Hemochromatosis gene nomenclature, AM J MED G, 93(1), 2000, pp. 77-77

Authors: Osborne, JP Jones, AC Burley, MW Jeganathan, D Young, J O'Callaghan, FJ Sampson, JR Povey, S
Citation: Jp. Osborne et al., Non-penetrance in tuberous sclerosis, LANCET, 355(9216), 2000, pp. 1698-1698

Authors: Wain, H Bruford, E Duncanson, A Lovering, R Povey, S
Citation: H. Wain et al., Nomenclature: Genes, weights and measures, animals, elements, and planets, RADIAT RES, 154(1), 2000, pp. 1-2

Authors: Lehmann, OJ Ebenezer, ND Jordan, T Fox, M Ocaka, L Payne, A Leroy, BP Clark, BJ Hitchings, RA Povey, S Khaw, PT Bhattacharya, SS
Citation: Oj. Lehmann et al., Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucoma, AM J HU GEN, 67(5), 2000, pp. 1129-1135

Authors: Lai, CSL Fisher, SE Hurst, JA Levy, ER Hodgson, S Fox, M Jeremiah, S Povey, S Jamison, DC Green, ED Vargha-Khadem, F Monaco, AP
Citation: Csl. Lai et al., The SPCH1 region on human 7q31: Genomic characterization of the critical interval and localization of translocations associated with speech and language disorder, AM J HU GEN, 67(2), 2000, pp. 357-368

Authors: Garibay-Tupas, JL Csiszar, K Fox, M Povey, S Bryant-Greenwood, GD
Citation: Jl. Garibay-tupas et al., Analysis of the 5 '-upstream regions of the human relaxin H1 and H2 genes and their chromosomal localization on chromosome 9p24.1 by radiation hybridand breakpoint mapping, J MOL ENDOC, 23(3), 1999, pp. 355-365

Authors: Wain, H White, J Povey, S
Citation: H. Wain et al., The changing challenges of nomenclature, CYTOG C GEN, 86(2), 1999, pp. 162-164

Authors: White, J Wain, H Bruford, E Povey, S
Citation: J. White et al., Promoting a standard nomenclature for genes and proteins, NATURE, 402(6760), 1999, pp. 347-347

Authors: Valente, EM Povey, S Warner, TT Wood, NW Davis, MB
Citation: Em. Valente et al., Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations, ANN HUM GEN, 63, 1999, pp. 1-8

Authors: Cox, DW Povey, S Shows, TB
Citation: Dw. Cox et al., Phyllis J. McAlpine, PhD, 1941-98: In memoriam - Obituary, AM J HU GEN, 64(4), 1999, pp. 1253-1254

Authors: Spurr, NK Cohen, D Adams, S Bakker, E Beckman, EJ Buys, CHCM Cann, HM Cassiman, JJ Contu, L Dixon, M Estivill, X Ferguson-Smith, MA Grzeschik, KH Hansmann, I Kruse, T McCarthy, T Moreno, F Moschonas, N Povey, S Roizes, G Terrenato, L Vergnaud, G Weissenbach, J Williamson, R Wright, A
Citation: Nk. Spurr et al., EUROGEM - Individual reports of all 23 network laboratories, BIOM HLTH R, 23, 1998, pp. 22-65

Authors: Wang, XH Fox, M Povey, S Masters, JRW
Citation: Xh. Wang et al., Mouse-human somatic cell hybrids: Loss of mouse and human chromosomes, SOM CELL M, 24(3), 1998, pp. 165-171
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