AAAAAA
Results:
1-7
|
Results: 7
Authors:
Dixon, M.J.
Read, A.P.
Donnai, D.
Colley, A.
Dixon, J.
Williamson, R.
Citation: Dixon, M.j et al., The gene for Treacher Collins syndrome maps to the long arm of chromosome 5., American journal of human genetics , 49-I(1), 1991, pp. 17-16
Authors:
Lathrop, G. M.
Farrall, M.
O'Connell, P.
Wainwright, B.
Leppert, M.
Nakamura, Y.
Lench, N.
Kruyer, H.
Dean, M.
Park, M.
Vande Woude, G.
Lalouel, I.-M.
Williamson, R.
White, R.
Citation: M. Lathrop, G. et al., Refined linkage map of chromosome 7 in the region of the cystic fibrosis gene, American journal of human genetics , 42(1), 1988, pp. 38-44
Authors:
Farrall, M.
Wainwright, B. J.
Feldman, G. L.
Beaudet, A.
Sretenovic, Z.
Halley, D.
Simon, M.
Dickerman, L.
Devoto, M.
Romeo, G.
Kaplan, J.-C.
Kitzis, A.
Williamson, R.
Citation: M. Farrall, et al., Recombinations between IRP and cystic fibrosis, American journal of human genetics , 43-II(4), 1988, pp. 471-475
Authors:
Keats, B. J. B.
Ward, L. J.
Krieger, M. Lu, S.
Wilensky, M. A.
Forster- Gibson, C. J.
Roy, M.
Monté, M.
Barbeau, A.
Simpson, N. E.
Eiberg, H.
Tippett, P.
Williamson, R.
Chamberlain, S.
Citation: B. Keats, B. J. et al., Linkage studies of friedreich ataxia by means of blood-group and protein markers, American journal of human genetics , 41-II(4), 1987, pp. 627-634
Authors:
Estivill, X.
McLean, C.
Nunes, V.
Casals, T.
Gallano, P.
Scambler, P.
Williamson, R.
Citation: X. Estivill, et al., Isolation of a new dna marker in linkage disequilibrium with cystic fibrosis, situated between J3.11 (D7S8) and IRP, American journal of human genetics , 44(5), 1989, pp. 704-710
Authors:
Tsilfidis, C.
MacKenzie, A. E.
Shutler, G.
Leblond, S.
Bailly, J.
Johnson, K.
Williamson, R.
Siegel-Bartelt, J.
Korneluk, R. G.
Shelbourne, P.
Citation: C. Tsilfidis, et al., D19S51 is closely linked with and maps distal to the myotonic dystrophy locus on 19q., American journal of human genetics , 49-II(5), 1991, pp. 961-965
Authors:
Johnson, K.
Shelbourne, P.
Davies, J.
Buxton, J.
Nimmo, E.
Siciliano, M. J.
Bachinski, L. L.
Anvret, M.
Harley, H.
Rundle, S.
Miki, T.
Brunner, H.
Williamson, R.
Citation: K. Johnson, et al., A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus, American journal of human genetics , 46-II(6), 1990, pp. 1073-1081
Risultati:
1-7
|