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Results: 1-5 |
Results: 5

Authors: Maddox, JF Davies, KP Crawford, AM Hulme, DJ Vaiman, D Cribiu, EP Freking, BA Beh, KJ Cockett, NE Kang, N Riffkin, CD Drinkwater, R Moore, SS Dodds, KG Lumsden, JM van Stijn, TC Phua, SH Adelson, DL Burkin, HR Broom, JE Buitkamp, J Cambridge, L Cushwa, WT Gerard, E Galloway, SM Harrison, B Hawken, RJ Hiendleder, S Henry, HM Medrano, JF Paterson, KA Schibler, L Stone, RT van Hest, B
Citation: Jf. Maddox et al., An enhanced linkage map of the sheep genome comprising more than 1000 loci, GENOME RES, 11(7), 2001, pp. 1275-1289

Authors: Dawkins, JL Hulme, DJ Brahmbhatt, SB Auer-Grumbach, M Nicholson, GA
Citation: Jl. Dawkins et al., Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain basesubunit-1, cause hereditary sensory neuropathy type I, NAT GENET, 27(3), 2001, pp. 309-312

Authors: Beh, KJ Callaghan, MJ Leish, Z Hulme, DJ Lenane, I Maddox, JF
Citation: Kj. Beh et al., A genome scan for QTL affecting fleece and wool traits in Merino sheep, WOOL TECH, 49(2), 2001, pp. 88-97

Authors: Nicholson, GA Dawkins, JL Blair, IP Auer-Grumbach, M Brahmbhatt, SB Hulme, DJ
Citation: Ga. Nicholson et al., Hereditary sensory neuropathy type I: Haplotype analysis shows founders insouthern England and Europe, AM J HU GEN, 69(3), 2001, pp. 655-659

Authors: Hulme, DJ Blair, IP Dawkins, JL Nicholson, GA
Citation: Dj. Hulme et al., Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis, HUM GENET, 106(6), 2000, pp. 594-596
Risultati: 1-5 |