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Results:
1-6
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Results: 6
Authors:
Suthers, G. K.
Hyland, V. J.
Callen, D. F.
Oberle, I.
Rocchi, M.
Thomas, N. S.
Morris, C. P.
Schwartz, C. E.
Schmidt, M.
Ropers, H. H.
Baker, E.
Oostra, B. A.
Dahl, N.
Wilson, P. J.
Hopwood, J.
Sutherland, G. R.
Citation: K. Suthers, G. et al., Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines, American journal of human genetics , 47-I(2), 1990, pp. 187-195
Authors:
Sutherland, G. R.
Jacky, P. B.
Baker, E.
Manuel, A.
Citation: R. Sutherland, G. et al., Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites:6p23,9p21, and 11q23, American journal of human genetics , 35(3), 1983, pp. 432-437
Authors:
Callen, D. F.
Freemantle, C. J.
Ringenbergs, M. L.
Baker, E.
Eyre, H. J.
Romain, D.
Haan, E. A.
Citation: F. Callen, D. et al., The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization., American journal of human genetics , 47-I(3), 1990, pp. 493-498
Authors:
Kremer, E. J.
Yu, S.
Pritchard, M.
Nagaraja, R.
Heitz, D.
Lynch, M.
Baker, E.
Hyland, V. J.
Little, R. D.
Wada, M.
Toniolo, D.
Vincent, A.
Rousseau, F.
Schlessinger, D.
Sutherland, G. R.
Richards, R. I.
Citation: J. Kremer, E. et al., Isolation of a human DNA sequence which spans the fragile X, American journal of human genetics , 49-I(3), 1991, pp. 656-661
Authors:
Scott, Hamish S.
Ashton, Lesley J.
Eyre, Helen J.
Baker, E.
Brooks, Doug A.
Callen, David F.
Sutherland, Grant R.
Morris, C. Phillip
Hopwood, John J.
Citation: S. Scott, Hamish et al., Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3., American journal of human genetics , 47-II(5), 1990, pp. 802-807
Authors:
Callen, D. F.
Baker, E.
Lane, S.
Nancarrow, J.
Thompson, A.
Whitmore, S. A.
MacLennan, D. H.
Berger, R.
Cherif, D.
Järvelä, I.
Peltonen, L.
Sutherland, G. R.
Gardiner, R. M.
Citation: F. Callen, D. et al., Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12, American journal of human genetics , 49-II(5), 1991, pp. 1372-1377
Risultati:
1-6
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