-
1
-
-
0029294082
-
The β and δ-thalassemia repository
-
BAYSAL, E. & M. F. H. CARVER. 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
-
2
-
-
85047689869
-
+-thalassemia-Portuguese type: Clinical, hematological and molecular studies of a newly defined form of β thalassemia
-
+-thalassemia-Portuguese type: clinical, hematological and molecular studies of a newly defined form of β thalassemia. Br. J. Haematol. 54: 189-200.
-
(1983)
Br. J. Haematol.
, vol.54
, pp. 189-200
-
-
Tamagnini, G.P.1
-
3
-
-
0023177954
-
The molecular basis of β-thalassemia in Lebanon: Application to prenatal diagnosis
-
CHEHAB, F. F. et al. 1987. The molecular basis of β-thalassemia in Lebanon: Application to prenatal diagnosis. Blood 69: 1141-1145.
-
(1987)
Blood
, vol.69
, pp. 1141-1145
-
-
Chehab, F.F.1
-
4
-
-
0023753296
-
Determination of the spectrum of β-thalassemia genes in Spain by use of dot-blot analysis of amplified β-globin DNA
-
AMSELEM, S. et al. 1988. Determination of the spectrum of β-thalassemia genes in Spain by use of dot-blot analysis of amplified β-globin DNA. Am. J. Hum. Genet. 43: 95-100.
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 95-100
-
-
Amselem, S.1
-
5
-
-
0024477306
-
A C→T substitution nt-101 in a conserved DNA sequence of the promoter region of the β-globin gene is associated with "silent" β-thalassemia
-
GONZALEZ-REDONDO, J. M. et al. 1989. A C→T substitution nt-101 in a conserved DNA sequence of the promoter region of the β-globin gene is associated with "silent" β-thalassemia. Blood 73: 1705-1711.
-
(1989)
Blood
, vol.73
, pp. 1705-1711
-
-
Gonzalez-Redondo, J.M.1
-
6
-
-
0025762515
-
Molecular characterization of β-thalassemia intermedia in patients of Italian descent and identification of three novel β-thalassemia mutations
-
MURRU, S. et al. 1991. Molecular characterization of β-thalassemia intermedia in patients of Italian descent and identification of three novel β-thalassemia mutations. Blood 77: 1342-1347.
-
(1991)
Blood
, vol.77
, pp. 1342-1347
-
-
Murru, S.1
-
7
-
-
85047692316
-
Thalassemia intermedia - The interaction of α and β-thalassemia
-
WAINSCOAT, J. S. et al. 1983. Thalassemia intermedia - the interaction of α and β-thalassemia. Br J Haematol 53: 411-416.
-
(1983)
Br J Haematol
, vol.53
, pp. 411-416
-
-
Wainscoat, J.S.1
-
8
-
-
0023741186
-
The molecular basis of thalassemia major and thalassemia intermedia in Asian Indians: Application to prenatal diagnosis
-
THEIN, S. L. et al. 1988. The molecular basis of thalassemia major and thalassemia intermedia in Asian Indians: application to prenatal diagnosis. Br. J. Haematol. 70: 225-231.
-
(1988)
Br. J. Haematol.
, vol.70
, pp. 225-231
-
-
Thein, S.L.1
-
9
-
-
0024338661
-
0-thalassemia intermedia in Sardinia
-
0-thalassemia intermedia in Sardinia. Blood 74: 823-827.
-
(1989)
Blood
, vol.74
, pp. 823-827
-
-
Galanello, R.1
-
10
-
-
0027204744
-
Increased HbF in adult life
-
WOOD, W. G. 1993: Increased HbF in adult life. Bailliere's Clin. Hematol. 6: 177-213.
-
(1993)
Bailliere's Clin. Hematol.
, vol.6
, pp. 177-213
-
-
Wood, W.G.1
-
11
-
-
0019401120
-
Localization of the site of recombination in formation of the Lepore Boston globin gene
-
BAIRD, M. et al. 1981. Localization of the site of recombination in formation of the Lepore Boston globin gene. J. Clin. Invest 68: 560.
-
(1981)
J. Clin. Invest
, vol.68
, pp. 560
-
-
Baird, M.1
-
12
-
-
0021172214
-
0-thalassemia in members of an American black family
-
0-thalassemia in members of an American black family. Blood 64: 941-944.
-
(1984)
Blood
, vol.64
, pp. 941-944
-
-
Padanilam, B.J.1
-
13
-
-
0022897892
-
Molecular characterization of an atypical β-thalassemia caused by a large deletion in the 5'β-globin gene region
-
POPOVITCH, B. W. et al. 1986. Molecular characterization of an atypical β-thalassemia caused by a large deletion in the 5'β-globin gene region. Am. J. Hum. Genet. 39: 797-810.
-
(1986)
Am. J. Hum. Genet.
, vol.39
, pp. 797-810
-
-
Popovitch, B.W.1
-
14
-
-
0023391977
-
An ∼300 bp deletion involving part of the 5'β-globin gene region is observed in members of a Turkish family with β-thalassemia
-
DIAZ-CHICO, J. C. et al. 1987. An ∼300 bp deletion involving part of the 5'β-globin gene region is observed in members of a Turkish family with β-thalassemia. Blood 70: 583-586.
-
(1987)
Blood
, vol.70
, pp. 583-586
-
-
Diaz-Chico, J.C.1
-
17
-
-
0028291289
-
Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassemia due to a homozygosity for the IVS 1-6 (T→C) mutation
-
EFREMOV, D. G. et al. 1994. Possible factors influencing the haemoglobin and fetal haemoglobin levels in patients with beta-thalassemia due to a homozygosity for the IVS 1-6 (T→C) mutation. Br. J. Haematol.
-
(1994)
Br. J. Haematol.
-
-
Efremov, D.G.1
-
18
-
-
0021355531
-
0-thalassemia in Sardinia
-
0-thalassemia in Sardinia Science 223: 924-930.
-
(1984)
Science
, vol.223
, pp. 924-930
-
-
Pirastu, M.1
-
19
-
-
0019518167
-
0-thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobin
-
0-thalassaemia and the Swiss type of hereditary persistence of fetal haemoglobin. Br J Haematol. 48: 561-572.
-
(1981)
Br J Haematol.
, vol.48
, pp. 561-572
-
-
Cappellini, M.D.1
Fiorelli, G.2
Bernini, L.F.3
-
20
-
-
0024780661
-
A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the β-globin gene complex
-
G. Stamatoyannopoulos & A. W. Nienhuis Eds.: Alan R Liss. New York
-
THEIN, S. L. & D. J. WEATHERALL. 1989. A non-deletion hereditary persistence of fetal hemoglobin (HPFH) determinant not linked to the β-globin gene complex. In Hemoglobin Switching. Part B: Cellular and Molecular Mechanisms. G. Stamatoyannopoulos & A. W. Nienhuis Eds.: 97-111. Alan R Liss. New York.
-
(1989)
Hemoglobin Switching. Part B: Cellular and Molecular Mechanisms
, pp. 97-111
-
-
Thein, S.L.1
Weatherall, D.J.2
-
21
-
-
0030065604
-
Dissecting the loci controlling fetal haemoglobin production on chromosomes 11p and 6q by the regressive approach
-
CRAIG, J. E. et al. 1996. Dissecting the loci 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
-
22
-
-
0026708201
-
Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2
-
DOVER, G. J. et al. 1992. Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2. Blood 80: 816-824.
-
(1992)
Blood
, vol.80
, pp. 816-824
-
-
Dover, G.J.1
-
23
-
-
0021067375
-
A family with segregating triplicated α-globin locus and β-thalassemia
-
GALANELLO, R. et al. 1983. A family with segregating triplicated α-globin locus and β-thalassemia. Blood 62: 1035-1040.
-
(1983)
Blood
, vol.62
, pp. 1035-1040
-
-
Galanello, R.1
-
24
-
-
85047693866
-
A benign form of thalassemia intermedia may be determined by the interaction of triplicated a locus and heterozygous β-thalassemia
-
CAMASCHELLA, C. et al. 1987. A benign form of thalassemia intermedia may be determined by the interaction of triplicated a locus and heterozygous β-thalassemia. Br. J. Haematol. 66: 103-107.
-
(1987)
Br. J. Haematol.
, vol.66
, pp. 103-107
-
-
Camaschella, C.1
-
25
-
-
0029964907
-
The triplicated α-globin gene locus in β-thalassemia heterozygotes: Clinical, haematological, biosynthetic and molecular studies
-
TRAEGER-SYNODINOS, J. et al. 1996. The triplicated α-globin gene locus in β-thalassemia heterozygotes: clinical, haematological, biosynthetic and molecular studies. Br. J. Haematol. 95: 467-471.
-
(1996)
Br. J. Haematol.
, vol.95
, pp. 467-471
-
-
Traeger-Synodinos, J.1
-
26
-
-
0025292312
-
Molecular basis of dominantly inherited inclusion body β-thalassemia
-
THEIN, S. L. et al. 1990. Molecular basis of dominantly inherited inclusion body β-thalassemia. Proc. Natl. Acad. Sci. USA 87: 3924-3928.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 3924-3928
-
-
Thein, S.L.1
-
27
-
-
0025053624
-
Silent β-thalassemia and thalassemia intermedia
-
HUISMAN, T. H. J. 1990. Silent β-thalassemia and thalassemia intermedia. Haematologica 75: 1-8.
-
(1990)
Haematologica
, vol.75
, pp. 1-8
-
-
Huisman, T.H.J.1
-
28
-
-
0024571738
-
0-thalassemia
-
0-thalassemia. Hemoglobin 13: 7-16.
-
(1989)
Hemoglobin
, vol.13
, pp. 7-16
-
-
Kutlar, A.1
|