-
1
-
-
0030221927
-
Mutation analysis in hereditary haemochromatosis
-
Beutler, E., Gelbart, T., West, C., Lee, P., Adams, M., Blackstone, R., Pockros, P., Kosty, M., Venditti, C.P., Phatak, P.D., Seese, N.K., Chorney, K.A., Elshof, A.E.T., Gerhard, G.S. & Chorney, M. (1996) Mutation analysis in hereditary haemochromatosis. Blood Cells, Molecules, and Diseases, 22, 187-194.
-
(1996)
Blood Cells, Molecules, and Diseases
, vol.22
, pp. 187-194
-
-
Beutler, E.1
Gelbart, T.2
West, C.3
Lee, P.4
Adams, M.5
Blackstone, R.6
Pockros, P.7
Kosty, M.8
Venditti, C.P.9
Phatak, P.D.10
Seese, N.K.11
Chorney, K.A.12
Elshof, A.E.T.13
Gerhard, G.S.14
Chorney, M.15
-
2
-
-
0030975526
-
Genetic detection of factor V Leiden: The question of specificity
-
Bowen, D.J. & Standen, G.R. (1997) Genetic detection of factor V Leiden: the question of specificity. British Journal of Haemotology, 97, 691-692.
-
(1997)
British Journal of Haemotology
, vol.97
, pp. 691-692
-
-
Bowen, D.J.1
Standen, G.R.2
-
3
-
-
0031059049
-
Genetic diagnosis of factor V Leiden using heteroduplex technology
-
Bowen, D.J., Standen, G.R., Granville, S., Bowley, S., Wood, N.A.P. & Bidwell, J. (1997) Genetic diagnosis of factor V Leiden using heteroduplex technology. Thrombosis and Haemostasis, 77, 119-122.
-
(1997)
Thrombosis and Haemostasis
, vol.77
, pp. 119-122
-
-
Bowen, D.J.1
Standen, G.R.2
Granville, S.3
Bowley, S.4
Wood, N.A.P.5
Bidwell, J.6
-
4
-
-
0006644568
-
Discontinuous polyacrylamide gel electrophoresis of DNA fragments
-
ed. by C. G. Mathew, Humana Press, New Jersey
-
Budowle, B. & Allen, R.C. (1991) Discontinuous polyacrylamide gel electrophoresis of DNA fragments. Protocols in Human Molecular Genetics (ed. by C. G. Mathew), p. 128. Humana Press, New Jersey.
-
(1991)
Protocols in Human Molecular Genetics
, pp. 128
-
-
Budowle, B.1
Allen, R.C.2
-
6
-
-
9344224529
-
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis
-
Feder, J.N., Gnirke, A., Thomas, W., Tsuchihashi, Z., Ruddy, D.A., Basava, A., Dormishian, F., Domingo, R., Ellis, M.C., Fullan, A., Hinton, L.M., Jones, N.L., Kimmel, G.S., Kronmal, G.S., Lauer, P., Lee, V.K., Loeb, D.B., Mapa, F.A., McClelland, E., Meyer, N.C., Mintier, G.A., Moeller, N., Moore, T., Morikang, E., Prass, C.E., Quintana, L., Starnes, S.M., Schatzman, R.C., Brunke, K.J., Drayna, D.T., Risch, N.J., Bacon, B.R. & Wolff, R.K. (1996) A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature Genetics, 13, 399-408.
-
(1996)
Nature Genetics
, vol.13
, pp. 399-408
-
-
Feder, J.N.1
Gnirke, A.2
Thomas, W.3
Tsuchihashi, Z.4
Ruddy, D.A.5
Basava, A.6
Dormishian, F.7
Domingo, R.8
Ellis, M.C.9
Fullan, A.10
Hinton, L.M.11
Jones, N.L.12
Kimmel, G.S.13
Kronmal, G.S.14
Lauer, P.15
Lee, V.K.16
Loeb, D.B.17
Mapa, F.A.18
McClelland, E.19
Meyer, N.C.20
Mintier, G.A.21
Moeller, N.22
Moore, T.23
Morikang, E.24
Prass, C.E.25
Quintana, L.26
Starnes, S.M.27
Schatzman, R.C.28
Brunke, K.J.29
Drayna, D.T.30
Risch, N.J.31
Bacon, B.R.32
Wolff, R.K.33
more..
-
7
-
-
0031092766
-
Putting a hold on HLA-'H'
-
Mercier, B., Mura, C., Ferec, C., Bodmer, J.G., Parham, P., Albert, E.D. & Marsh, S.G.E. (1997) Putting a hold on HLA-'H'. Nature Genetics, 15, 234-235.
-
(1997)
Nature Genetics
, vol.15
, pp. 234-235
-
-
Mercier, B.1
Mura, C.2
Ferec, C.3
Bodmer, J.G.4
Parham, P.5
Albert, E.D.6
Marsh, S.G.E.7
-
8
-
-
0030923653
-
Global prevalence of putative haemochromatosis mutations
-
Merryweather-Clarke, A.T., Pointon, J.J., Shearman, J.D. & Robson, K.J.H. (1997) Global prevalence of putative haemochromatosis mutations. Journal of Medical Genetics, 34, 275-278.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 275-278
-
-
Merryweather-Clarke, A.T.1
Pointon, J.J.2
Shearman, J.D.3
Robson, K.J.H.4
-
9
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller, S.A., Dykes, D.D. & Polesky, H.F. (1986) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleci Acids Research, 16, 1215.
-
(1986)
Nucleci Acids Research
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
10
-
-
0029998864
-
UHG-based mutation screening in type 2B von Willebrands disease: Detection of a candidate mutation in Ser547Phe
-
Wood, N., Standen, G.R., Bowen, D.J., Worming, A., Lush, C., Lee, R. & Bidwell, J. (1996) UHG-based mutation screening in type 2B von Willebrands disease: detection of a candidate mutation in Ser547Phe. Thrombosis and Haemostasis, 75, 363-367.
-
(1996)
Thrombosis and Haemostasis
, vol.75
, pp. 363-367
-
-
Wood, N.1
Standen, G.R.2
Bowen, D.J.3
Worming, A.4
Lush, C.5
Lee, R.6
Bidwell, J.7
-
11
-
-
0027370957
-
Diagnosis of sickle-cell disease with a universal heteroduplex generator
-
Wood, N., Standen, G.R., Hows, J., Bradley, B. & Bidwell, J. (1993) Diagnosis of sickle-cell disease with a universal heteroduplex generator. Lancet, 342, 1519.
-
(1993)
Lancet
, vol.342
, pp. 1519
-
-
Wood, N.1
Standen, G.R.2
Hows, J.3
Bradley, B.4
Bidwell, J.5
-
13
-
-
0005600868
-
A simple genetic test identifies 90% of UK patients with haemochromatosis
-
in press
-
Worwood M., Shearman, J.D., Wallace, D.S., Dooley, J., Merryweather-Clarke, A.T., Pointon, J.-J., Rosenberg, W.M.C., Bowen, D.J., Burnett, A.K., Jackson, H.A., Lawless, S., Rahe-Chourdhury, R., Partridge, J., Williams, R., Bomford, A., Walker, A.P. & Robson, K.J.H. (1997) A simple genetic test identifies 90% of UK patients with haemochromatosis. Gut, in press.
-
(1997)
Gut
-
-
Worwood, M.1
Shearman, J.D.2
Wallace, D.S.3
Dooley, J.4
Merryweather-Clarke, A.T.5
Pointon, J.-J.6
Rosenberg, W.M.C.7
Bowen, D.J.8
Burnett, A.K.9
Jackson, H.A.10
Lawless, S.11
Rahe-Chourdhury, R.12
Partridge, J.13
Williams, R.14
Bomford, A.15
Walker, A.P.16
Robson, K.J.H.17
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