-
1
-
-
0022627617
-
+ thalassemia intermedia associated with δ° thalassemia
-
+ thalassemia intermedia associated with δ° thalassemia. Blood, 67, 957-961.
-
(1986)
Blood
, vol.67
, pp. 957-961
-
-
Baklouti, F.1
Dorleac, E.2
Morle, L.3
Laselve, P.4
Peyramond, D.5
Aubry, M.6
Godet, J.7
Delaunay, J.8
-
2
-
-
0029294082
-
The β- and δ-thalassemia repository
-
Baysal, E. & Carver, M.F.H. (1995) The β- and δ-thalassemia repository. Hemoglobin, 19, 213-236.
-
(1995)
Hemoglobin
, vol.19
, pp. 213-236
-
-
Baysal, E.1
Carver, M.F.H.2
-
3
-
-
85047693866
-
A benign form of thalassaemia intermedia may be determined by the interaction of triplicated α locus and heterozygous β-thalassaemia
-
Camaschella, C., Bertero, M.T., Serra, A., Dall'Acqua, M., Gasparini, P., Trento, M., Vettore, L., Perona, G., Saglio, G. & Mazza, U. (1987) A benign form of thalassaemia intermedia may be determined by the interaction of triplicated α locus and heterozygous β-thalassaemia. British Journal of Haematology, 66, 103-107.
-
(1987)
British Journal of Haematology
, vol.66
, pp. 103-107
-
-
Camaschella, C.1
Bertero, M.T.2
Serra, A.3
Dall'Acqua, M.4
Gasparini, P.5
Trento, M.6
Vettore, L.7
Perona, G.8
Saglio, G.9
Mazza, U.10
-
4
-
-
0028942051
-
Genetic interactions in thalassemia intermedia: Analysis of β-mutations. α-genotype, γ-promoters, and β-LCR hypersensitive sites 2 and 4 in Italian patients
-
Camaschella, C., Maza, U., Roetto, A., Gottardi, E., Parziale, A., Travi, M., Fattore, S., Bacchiega, D., Fiorelli, G. & Cappellini, M.D. (1995) Genetic interactions in thalassemia intermedia: analysis of β-mutations. α-genotype, γ-promoters, and β-LCR hypersensitive sites 2 and 4 in Italian patients. American Journal of Hematology, 48, 82-87.
-
(1995)
American Journal of Hematology
, vol.48
, pp. 82-87
-
-
Camaschella, C.1
Maza, U.2
Roetto, A.3
Gottardi, E.4
Parziale, A.5
Travi, M.6
Fattore, S.7
Bacchiega, D.8
Fiorelli, G.9
Cappellini, M.D.10
-
5
-
-
0023177954
-
The molecular basis of β-thalassemia in Lebanon: Application of prenatal diagnosis
-
Chehab, F.F., Der Kaloustian, V., Khouri, F.P., Deeb, S.S. & Kan, Y.W. (1987) The molecular basis of β-thalassemia in Lebanon: application of prenatal diagnosis. Blood. 69, 1141-1145.
-
(1987)
Blood
, vol.69
, pp. 1141-1145
-
-
Chehab, F.F.1
Der Kaloustian, V.2
Khouri, F.P.3
Deeb, S.S.4
Kan, Y.W.5
-
6
-
-
0014404927
-
Separation of the alpha and beta chains of human haemoglobin
-
Clegg, J.B., Naughton, M.A. & Weatherall, D.J. (1968) Separation of the alpha and beta chains of human haemoglobin. Nature, 219, 69-70.
-
(1968)
Nature
, vol.219
, pp. 69-70
-
-
Clegg, J.B.1
Naughton, M.A.2
Weatherall, D.J.3
-
7
-
-
0030065604
-
Dissecting the Ioci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach
-
Craig, J.E., Rochette, J., Fisher, C.A., Weatherall, D.J., Marc, S., Lathrop, G.M., Demenais, F. & Thein, S.L. (1996) Dissecting the Ioci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach. Nature Genetics, 12, 58-64.
-
(1996)
Nature Genetics
, vol.12
, pp. 58-64
-
-
Craig, J.E.1
Rochette, J.2
Fisher, C.A.3
Weatherall, D.J.4
Marc, S.5
Lathrop, G.M.6
Demenais, F.7
Thein, S.L.8
-
8
-
-
0027300074
-
The molecular basis of HPFH in a British family identified by heteroduplex formation
-
Craig, J.E., Sheerin, S.M., Barnetson, R. & Thein, S.L. (1993) The molecular basis of HPFH in a British family identified by heteroduplex formation. British Journal of Haematology, 84, 106-110.
-
(1993)
British Journal of Haematology
, vol.84
, pp. 106-110
-
-
Craig, J.E.1
Sheerin, S.M.2
Barnetson, R.3
Thein, S.L.4
-
9
-
-
0023840728
-
Mild and severe β-thalassemia among homozygotes from Turkey: Identification of the types by hybridization of amplified DNA with synthetic probes
-
Diaz-Chico, J.C., Yang, K.G., Stoming, T.A., Efremov, D.G., Kutlar, A., Kutlar, F. Aksoy, M., Altay, C., Gurgey, A., Kilinc, Y. & Huisman, T.H.J. (1988) Mild and severe β-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes. Blood, 71, 248-251.
-
(1988)
Blood
, vol.71
, pp. 248-251
-
-
Diaz-Chico, J.C.1
Yang, K.G.2
Stoming, T.A.3
Efremov, D.G.4
Kutlar, A.5
Kutlar, F.6
Aksoy, M.7
Altay, C.8
Gurgey, A.9
Kilinc, Y.10
Huisman, T.H.J.11
-
10
-
-
0024338661
-
Molecular analysis of β°-thalassemia intermedia in Sardinia
-
Galanello, R., Dessi, E., Melis, M.A., Addis, M., Sanna, M.A., Rosatelli, C., Argiolu, F., Glagu, N., Turco, M.P., Cacace, E., Pirastu, M.M. & Cao, A. (1989) Molecular analysis of β°-thalassemia intermedia in Sardinia. Blood, 74, 823-827.
-
(1989)
Blood
, vol.74
, pp. 823-827
-
-
Galanello, R.1
Dessi, E.2
Melis, M.A.3
Addis, M.4
Sanna, M.A.5
Rosatelli, C.6
Argiolu, F.7
Glagu, N.8
Turco, M.P.9
Cacace, E.10
Pirastu, M.M.11
Cao, A.12
-
11
-
-
0027018911
-
A comprehensive scanning method for rapid detection of β globin gene mutations and polymorphisms
-
Ghanem, N., Girodon, E., Vidaud, M., Martin, J., Fanen, P., Plassa, F. & Goossens, M. (1992) A comprehensive scanning method for rapid detection of β globin gene mutations and polymorphisms. Human Mutations, 1, 229.
-
(1992)
Human Mutations
, vol.1
, pp. 229
-
-
Ghanem, N.1
Girodon, E.2
Vidaud, M.3
Martin, J.4
Fanen, P.5
Plassa, F.6
Goossens, M.7
-
12
-
-
0020985678
-
A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster
-
Gianni, A.M., Bregni, M., Cappellini, M.D., Fiorelli, G., Taramelli, R., Giglioni, B., Comi, P. & Ottolenghi, S. (1983) A gene controlling fetal hemoglobin expression in adults is not linked to the non-α globin cluster. EMBO Journal, 2, 921-925.
-
(1983)
EMBO Journal
, vol.2
, pp. 921-925
-
-
Gianni, A.M.1
Bregni, M.2
Cappellini, M.D.3
Fiorelli, G.4
Taramelli, R.5
Giglioni, B.6
Comi, P.7
Ottolenghi, S.8
-
14
-
-
0026443778
-
Beta thalassaemia in the indigenous British population
-
Hall, G.W., Barnetson, R.A. & Thein, S.L. (1992) Beta thalassaemia in the indigenous British population. British Journal of Haematology, 82, 584.
-
(1992)
British Journal of Haematology
, vol.82
, pp. 584
-
-
Hall, G.W.1
Barnetson, R.A.2
Thein, S.L.3
-
15
-
-
0026043736
-
A novel mutation (nonsense β127) in exon 3 of the β globin gene produces a variable thalassaemia phenotype
-
Hall, G.W., Franklin, I.M., Sura, T. & Thein, S.L. (1991) A novel mutation (nonsense β127) in exon 3 of the β globin gene produces a variable thalassaemia phenotype. British Journal of Haematology, 79, 342-344.
-
(1991)
British Journal of Haematology
, vol.79
, pp. 342-344
-
-
Hall, G.W.1
Franklin, I.M.2
Sura, T.3
Thein, S.L.4
-
16
-
-
0030023834
-
Moderate reduction of β globin gene transcript by a novel mutation in the 5′ untranslated region: A study of its interaction with other genotypes in two families
-
Ho, P.J., Rochette, J., Fisher, C.A., Wonke, B., Jarvis, M.K., Yardumian, A. & Thein, S.L. (1996) Moderate reduction of β globin gene transcript by a novel mutation in the 5′ untranslated region: a study of its interaction with other genotypes in two families. Blood, 87, 1170-1178.
-
(1996)
Blood
, vol.87
, pp. 1170-1178
-
-
Ho, P.J.1
Rochette, J.2
Fisher, C.A.3
Wonke, B.4
Jarvis, M.K.5
Yardumian, A.6
Thein, S.L.7
-
17
-
-
85047689933
-
Thalassaemia intermedia: Interaction of the triple α-globin gene arrangement and heterozygous β thalassaemia
-
Kulozik, A.E., Thein, S.L., Wainscoat, J.S., Gale, R., Kay, L.A., Wood, J.K., Weatherall, D.J. & Huehns, E.R. (1987) Thalassaemia intermedia: interaction of the triple α-globin gene arrangement and heterozygous β thalassaemia. British Journal of Haematology, 66, 109-112.
-
(1987)
British Journal of Haematology
, vol.66
, pp. 109-112
-
-
Kulozik, A.E.1
Thein, S.L.2
Wainscoat, J.S.3
Gale, R.4
Kay, L.A.5
Wood, J.K.6
Weatherall, D.J.7
Huehns, E.R.8
-
18
-
-
0346497365
-
Gγ-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients
-
Gγ-globin gene expression and high Hb F levels in β-thalassemia and sickle cell anemia patients. Proceedings of the National Academy of Sciences of the United States of America, 82, 2111-2114.
-
(1985)
Proceedings of the National Academy of Sciences of the United States of America
, vol.82
, pp. 2111-2114
-
-
Labie, D.1
Pagnier, J.2
Lapoumeroulie, C.3
Rouabhi, F.4
Dunda-Belkhodja, O.5
Chardin, P.6
Beldjord, C.7
Wajcman, H.8
Fabry, M.E.9
Nagel, R.L.10
-
19
-
-
0026569366
-
Promoter mutations producing mild β-thalassaemia in the Italian population
-
Meloni, A., Rosatelli, M.C., Faa, V., Sardu, R., Saba, L., Murru, S., Sciarratta, G.V., Baldi, M. & Tannoia, N. (1992) Promoter mutations producing mild β-thalassaemia in the Italian population. British Journal of Haematology, 80, 222-226.
-
(1992)
British Journal of Haematology
, vol.80
, pp. 222-226
-
-
Meloni, A.1
Rosatelli, M.C.2
Faa, V.3
Sardu, R.4
Saba, L.5
Murru, S.6
Sciarratta, G.V.7
Baldi, M.8
Tannoia, N.9
-
20
-
-
0026723551
-
A β-thalassaemia phenotype not linked to the β-globin cluster in an Italian family
-
Murru, S., Loudianos, G., Porcu, S., Sciarratta, G.V., Agosli, S., Parodi, M.I., Cao, A. & Pirastu, M. (1992) A β-thalassaemia phenotype not linked to the β-globin cluster in an Italian family. British Journal of Haematology, 81, 283-287.
-
(1992)
British Journal of Haematology
, vol.81
, pp. 283-287
-
-
Murru, S.1
Loudianos, G.2
Porcu, S.3
Sciarratta, G.V.4
Agosli, S.5
Parodi, M.I.6
Cao, A.7
Pirastu, M.8
-
21
-
-
0025090944
-
Rapid detection and prenatal diagnosis of β-thalassaemia: Studies in Indian and Cypriot populations in the UK
-
Old, J.M., Varawalla, N.Y. & Weatherall, D.J. (1990) Rapid detection and prenatal diagnosis of β-thalassaemia: studies in Indian and Cypriot populations in the UK. Lancet, 336, 834-837.
-
(1990)
Lancet
, vol.336
, pp. 834-837
-
-
Old, J.M.1
Varawalla, N.Y.2
Weatherall, D.J.3
-
22
-
-
0025923084
-
A novel δ° mutation in cis with Hb Knossos: A study of different genetic interactions in three Egyptian families
-
Olds, R.J., Sura, T., Jackson, B., Wonke, B., Hoffbrand, A.V. & Thein, S.L. (1991) A novel δ° mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families. British Journal of Haematology, 78, 430-436.
-
(1991)
British Journal of Haematology
, vol.78
, pp. 430-436
-
-
Olds, R.J.1
Sura, T.2
Jackson, B.3
Wonke, B.4
Hoffbrand, A.V.5
Thein, S.L.6
-
23
-
-
0019949838
-
Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster
-
Orkin, S.H., Kazazian, H.H.J., Antonarakis, S.E., Goff, S.C., Boehm, C.D., Sexton, J.P., Waber, P.G. & Giardina, P.J.V. (1982) Linkage of β-thalassaemia mutations and β-globin gene polymorphisms with DNA polymorphisms in human β-globin gene cluster. Nature, 296, 627-631.
-
(1982)
Nature
, vol.296
, pp. 627-631
-
-
Orkin, S.H.1
Kazazian, H.H.J.2
Antonarakis, S.E.3
Goff, S.C.4
Boehm, C.D.5
Sexton, J.P.6
Waber, P.G.7
Giardina, P.J.V.8
-
24
-
-
0028247096
-
Severe thalassaemia intermedia caused by interaction of homozygosity for α-globin gene triplication with heterozygosity for β°-thalassaemia
-
Oron, V., Filon, D., Oppenheim, A. & Rund, D. (1994) Severe thalassaemia intermedia caused by interaction of homozygosity for α-globin gene triplication with heterozygosity for β°-thalassaemia. British Journal of Haematology, 86, 377-379.
-
(1994)
British Journal of Haematology
, vol.86
, pp. 377-379
-
-
Oron, V.1
Filon, D.2
Oppenheim, A.3
Rund, D.4
-
25
-
-
0025194949
-
The C→T substitution in the distal CACCC box of the β-globin gene promoter is a common cause of silent β thalassaemia in the Italian population
-
Ristaldi, M.S., Murru, S., Loudianos, G., Casula, L., Porcu, S., Pigheddu, D., Fanni, B., Sciaratta, G.V., Agosti, S., Parodi, M.I., Leone, D., Camaschella, C., Serra, A., Pirastu, M. & Cao, A. (1990) The C→T substitution in the distal CACCC box of the β-globin gene promoter is a common cause of silent β thalassaemia in the Italian population. British Journal of Haematology, 74, 480-486.
-
(1990)
British Journal of Haematology
, vol.74
, pp. 480-486
-
-
Ristaldi, M.S.1
Murru, S.2
Loudianos, G.3
Casula, L.4
Porcu, S.5
Pigheddu, D.6
Fanni, B.7
Sciaratta, G.V.8
Agosti, S.9
Parodi, M.I.10
Leone, D.11
Camaschella, C.12
Serra, A.13
Pirastu, M.14
Cao, A.15
-
26
-
-
0031012244
-
Genetic analysis of β-thalassaemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
-
Rund, D., Oron-Karni, V., Filon, D., Goldfarb, A., Rachmilewitz, E. & Oppenheim, A. (1997) Genetic analysis of β-thalassaemia intermedia in Israel: diversity of mechanisms and unpredictability of phenotype. American Journal of Hematology, 54, 16-22.
-
(1997)
American Journal of Hematology
, vol.54
, pp. 16-22
-
-
Rund, D.1
Oron-Karni, V.2
Filon, D.3
Goldfarb, A.4
Rachmilewitz, E.5
Oppenheim, A.6
-
28
-
-
0007699586
-
Haemoglobin analysis
-
ed. by I. Chanarin. Churchill Livingstone, Edinburgh
-
Sharpe, J.A. & Wood, W.G. (1989) Haemoglobin analysis. Laboratory Haematology (ed. by I. Chanarin). pp. 33-54. Churchill Livingstone, Edinburgh.
-
(1989)
Laboratory Haematology
, pp. 33-54
-
-
Sharpe, J.A.1
Wood, W.G.2
-
29
-
-
85047689869
-
+ Thalassaemia Portuguese type: Clinical, haematological and molecular studies of a newly defined form of β thalassaemia
-
+ Thalassaemia Portuguese type: clinical, haematological and molecular studies of a newly defined form of β thalassaemia. British Journal of Haematology, 54, 189-200.
-
(1983)
British Journal of Haematology
, vol.54
, pp. 189-200
-
-
Tamagnini, G.P.1
Lopes, M.C.2
Castanheira, M.E.3
Wainscoat, J.S.4
-
31
-
-
0025856898
-
Hemoglobin Chesterfield (β28 Leu→Arg) produces the phenotype of inclusion body β thalassemia
-
Thein, S.L., Best, S., Sharpe, J., Paul, B., Clark, D.J. & Brown, M.J. (1991) Hemoglobin Chesterfield (β28 Leu→Arg) produces the phenotype of inclusion body β thalassemia. Blood, 77, 2791-2793.
-
(1991)
Blood
, vol.77
, pp. 2791-2793
-
-
Thein, S.L.1
Best, S.2
Sharpe, J.3
Paul, B.4
Clark, D.J.5
Brown, M.J.6
-
32
-
-
0001788530
-
The use of synthetic oligonucleotides as specific hybridization probes in the diagnosis of genetic disorders
-
ed. by K. E. Davies, IRL Press, Oxford
-
Thein, S.L., Ehsani, A. & Wallace, R.B. (1993a) The use of synthetic oligonucleotides as specific hybridization probes in the diagnosis of genetic disorders. Human Genetic Disease Analysis: a Practical Approach (ed. by K. E. Davies), pp. 21-33. IRL Press, Oxford.
-
(1993)
Human Genetic Disease Analysis: A Practical Approach
, pp. 21-33
-
-
Thein, S.L.1
Ehsani, A.2
Wallace, R.B.3
-
33
-
-
0025292312
-
Molecular basis for dominantly inherited inclusion body β-thalassemia
-
Thein, S.L., Hesketh, C., Taylor, P., Temperley, I.J., Hutchinson, R.M., Old, J.M., Wood, W.G., Clegg, J.B. & Weatherall, D.J. (1990) Molecular basis for dominantly inherited inclusion body β-thalassemia. Proceedings of the National Academy of Sciences of the United States of America, 87, 3924-3928.
-
(1990)
Proceedings of the National Academy of Sciences of the United States of America
, vol.87
, pp. 3924-3928
-
-
Thein, S.L.1
Hesketh, C.2
Taylor, P.3
Temperley, I.J.4
Hutchinson, R.M.5
Old, J.M.6
Wood, W.G.7
Clegg, J.B.8
Weatherall, D.J.9
-
34
-
-
0023741186
-
The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: Application to prenatal diagnosis
-
Thein, S.L., Hesketh, C., Wallace, R.B. & Weatherall, D.J. (1988) The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis. British Journal of Haematology, 70, 225-231.
-
(1988)
British Journal of Haematology
, vol.70
, pp. 225-231
-
-
Thein, S.L.1
Hesketh, C.2
Wallace, R.B.3
Weatherall, D.J.4
-
35
-
-
0025993003
-
A simple and rapid method of direct sequencing using Dynabeads
-
Thein, S.L. & Hinton, J. (1991) A simple and rapid method of direct sequencing using Dynabeads. British Journal of Haematology. 79, 113-115.
-
(1991)
British Journal of Haematology
, vol.79
, pp. 113-115
-
-
Thein, S.L.1
Hinton, J.2
-
36
-
-
0028012604
-
Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers
-
Thein, S.L., Sampietro, M., Rohde, K., Rochette, J., Weatherall, D.J., Lathrop, G.M. & Demenais, F. (1994) Detection of a major gene for heterocellular hereditary persistence of fetal hemoglobin after accounting for genetic modifiers. American Journal of Human Genetics, 54, 214-228.
-
(1994)
American Journal of Human Genetics
, vol.54
, pp. 214-228
-
-
Thein, S.L.1
Sampietro, M.2
Rohde, K.3
Rochette, J.4
Weatherall, D.J.5
Lathrop, G.M.6
Demenais, F.7
-
37
-
-
0023158314
-
Association of thalassaemia intermedia with a beta-globin gene haplotype
-
Thein, S.L., Wainscoat, J.S., Sampietro, M., Old, J.M., Cappellini, D., Fiorelli, G., Modell, B. & Weatherall, D.J. (1987) Association of thalassaemia intermedia with a beta-globin gene haplotype. British Journal of Haematology, 65, 367-373.
-
(1987)
British Journal of Haematology
, vol.65
, pp. 367-373
-
-
Thein, S.L.1
Wainscoat, J.S.2
Sampietro, M.3
Old, J.M.4
Cappellini, D.5
Fiorelli, G.6
Modell, B.7
Weatherall, D.J.8
-
38
-
-
0027202405
-
β-Thalassemia unlinked to the β-globin gene in an English family
-
Thein, S.L., Wood, W.G., Wickramasinghe, S.N. & Galvin, M.C. (1993b) β-Thalassemia unlinked to the β-globin gene in an English family. Blood, 82, 961-957.
-
(1993)
Blood
, vol.82
, pp. 961-1957
-
-
Thein, S.L.1
Wood, W.G.2
Wickramasinghe, S.N.3
Galvin, M.C.4
-
39
-
-
0028305957
-
Immunochemical estimation of haemoglobin types in red blood cells by FACS analysis
-
Thorpe, S.J., Thein, S.L., Sampietro, M., Craig, J.E., Mahon, B. & Huehns, E.R. (1994) Immunochemical estimation of haemoglobin types in red blood cells by FACS analysis. British Journal of Haematology, 87, 125-132.
-
(1994)
British Journal of Haematology
, vol.87
, pp. 125-132
-
-
Thorpe, S.J.1
Thein, S.L.2
Sampietro, M.3
Craig, J.E.4
Mahon, B.5
Huehns, E.R.6
-
40
-
-
85047692316
-
Thalassaemia intermedia in Cyprus: The interaction of α and β-thalassaemia
-
Wainscoat, J.S., Kanavakis, E., Wood, W.G., Letsky, E.A., Huehns, E.R., Marsh, G.W., Higgs, D.R., Clegg, J.B. & Weatherall, D.J. (1983) Thalassaemia intermedia in Cyprus: the interaction of α and β-thalassaemia. British Journal of Haematology, 53, 411-416.
-
(1983)
British Journal of Haematology
, vol.53
, pp. 411-416
-
-
Wainscoat, J.S.1
Kanavakis, E.2
Wood, W.G.3
Letsky, E.A.4
Huehns, E.R.5
Marsh, G.W.6
Higgs, D.R.7
Clegg, J.B.8
Weatherall, D.J.9
-
42
-
-
0024592813
-
β-Thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the β-globin gene
-
Wong, C., Antonarakis, S.E., Goff, S.C., Orkin, S.H., Forget, B.G., Nathan, D.G., Giardina, P.J.V. & Kazazian, H.H.J. (1989) β-Thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the β-globin gene. Blood, 73, 914-918.
-
(1989)
Blood
, vol.73
, pp. 914-918
-
-
Wong, C.1
Antonarakis, S.E.2
Goff, S.C.3
Orkin, S.H.4
Forget, B.G.5
Nathan, D.G.6
Giardina, P.J.V.7
Kazazian, H.H.J.8
-
43
-
-
0023601968
-
Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA
-
Wong, C., Dowling, C.E., Saiki, R.K., Higuchi, R.G., Erlich, H.A. & Kazazian, H.H.J. (1987) Characterization of β-thalassaemia mutations using direct genomic sequencing of amplified single copy DNA, Nature, 330, 384-386.
-
(1987)
Nature
, vol.330
, pp. 384-386
-
-
Wong, C.1
Dowling, C.E.2
Saiki, R.K.3
Higuchi, R.G.4
Erlich, H.A.5
Kazazian, H.H.J.6
-
44
-
-
0024588742
-
Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major
-
Yang, K.G., Kutlar, F., George, E., Wilson, J.B., Kutlar, A., Stoming, T.A., Gonzalez-Redondo, J.M. & Huisman, T.H.J. (1989) Molecular characterization of β-globin gene mutations in Malay patients with Hb E-β-thalassaemia and thalassaemia major. British Journal of Haematology, 72, 73.
-
(1989)
British Journal of Haematology
, vol.72
, pp. 73
-
-
Yang, K.G.1
Kutlar, F.2
George, E.3
Wilson, J.B.4
Kutlar, A.5
Stoming, T.A.6
Gonzalez-Redondo, J.M.7
Huisman, T.H.J.8
|