-
2
-
-
20044391420
-
Heterogeneity of the εγδβ-thalassaemias: Characterization of three novel English deletions
-
Rooks H, Bergounioux J, Game L, et al. Heterogeneity of the εγδβ-thalassaemias: Characterization of three novel English deletions. Br J Haematol 2005;128:722-729.
-
(2005)
Br J Haematol
, vol.128
, pp. 722-729
-
-
Rooks, H.1
Bergounioux, J.2
Game, L.3
-
3
-
-
0030038097
-
A de novo deletion causing εγδβ-thalassemia in a Dutch patient
-
Abels J, Michiels JJ, Giordano PC, et al. A de novo deletion causing εγδβ-thalassemia in a Dutch patient. Acta Haematol 1996;96:108-109.
-
(1996)
Acta Haematol
, vol.96
, pp. 108-109
-
-
Abels, J.1
Michiels, J.J.2
Giordano, P.C.3
-
4
-
-
0141818962
-
A novel deletion causing (εγδβ)0 thalassaemia in a Chilean family
-
Game L, Bergounioux J, Close JP, et al. A novel deletion causing (εγδβ)0 thalassaemia in a Chilean family. Br J Haematol 2003;123:154-159.
-
(2003)
Br J Haematol
, vol.123
, pp. 154-159
-
-
Game, L.1
Bergounioux, J.2
Close, J.P.3
-
5
-
-
0041410228
-
Novel 112 kb (eGgAg)db-thalassaemia deletion in a Dutch family
-
Harteveld CL, Osborne CS, Peters M, et al. Novel 112 kb (eGgAg)db-thalassaemia deletion in a Dutch family. Br J Haematol 2003;122:855-858.
-
(2003)
Br J Haematol
, vol.122
, pp. 855-858
-
-
Harteveld, C.L.1
Osborne, C.S.2
Peters, M.3
-
6
-
-
0012953756
-
γδβ-thalassemia due to a de novo mutation deleting the 5′ β-globin gene activation-region hypersensitive sites
-
Driscoll MC, Dobkin CS, Alter BP. γδβ-thalassemia due to a de novo mutation deleting the 5′ β-globin gene activation-region hypersensitive sites. Proc Natl Acad Sci USA 1989;86:7470-7474.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 7470-7474
-
-
Driscoll, M.C.1
Dobkin, C.S.2
Alter, B.P.3
-
7
-
-
0023677752
-
Two new large deletions resulting in εγδβ-thalassemia
-
Diaz-Chico JC, Huang HJ, Juricic D, et al. Two new large deletions resulting in εγδβ-thalassemia. Acta Haematol 1988;80:79-84.
-
(1988)
Acta Haematol
, vol.80
, pp. 79-84
-
-
Diaz-Chico, J.C.1
Huang, H.J.2
Juricic, D.3
-
8
-
-
0020567504
-
The entire β-globin gene cluster is deleted in a form of γδβ-thalassemia
-
Fearon ER, Kazazian HH Jr, Waber PG, et al. The entire β-globin gene cluster is deleted in a form of γδβ-thalassemia. Blood 1983;61:1269-1274.
-
(1983)
Blood
, vol.61
, pp. 1269-1274
-
-
Fearon, E.R.1
Kazazian Jr, H.H.2
Waber, P.G.3
-
9
-
-
0025844863
-
A greater than 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish descent
-
Fortina P, Delgrosso K, Werner E, et al. A greater than 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish descent. Hemoglobin 1991;15:23-41.
-
(1991)
Hemoglobin
, vol.15
, pp. 23-41
-
-
Fortina, P.1
Delgrosso, K.2
Werner, E.3
-
10
-
-
0023647951
-
Recombination at the human α-globin gene cluster: Sequence features and topological constraints
-
Nicholls RD, Fischel-Ghodsian N, Higgs DR. Recombination at the human α-globin gene cluster: Sequence features and topological constraints. Cell 1987;49:369-378.
-
(1987)
Cell
, vol.49
, pp. 369-378
-
-
Nicholls, R.D.1
Fischel-Ghodsian, N.2
Higgs, D.R.3
-
11
-
-
23244468467
-
A novel GγAγ (δβ)0-thalassemia with a 27 kb deletion
-
Yamashiro Y, Hattori Y, Okayama N, et al. A novel GγAγ (δβ)0-thalassemia with a 27 kb deletion. Hemoglobin 2005;29:197-208.
-
(2005)
Hemoglobin
, vol.29
, pp. 197-208
-
-
Yamashiro, Y.1
Hattori, Y.2
Okayama, N.3
-
13
-
-
0025223668
-
Molecular and hematologic characterization of Scottish-Irish type (εγδβ)0 thalassemia
-
Trent RJ, Williams BG, Kearney A, et al. Molecular and hematologic characterization of Scottish-Irish type (εγδβ)0 thalassemia. Blood 1990;76:2132-2138.
-
(1990)
Blood
, vol.76
, pp. 2132-2138
-
-
Trent, R.J.1
Williams, B.G.2
Kearney, A.3
-
14
-
-
0030850053
-
Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia
-
Camaschella C, Kattamis AC, Petroni D, et al. Different hematological phenotypes caused by the interaction of triplicated α-globin genes and heterozygous β-thalassemia. Am J Hematol 1997;55:83-88.
-
(1997)
Am J Hematol
, vol.55
, pp. 83-88
-
-
Camaschella, C.1
Kattamis, A.C.2
Petroni, D.3
-
15
-
-
38349070438
-
-
Hattori Y, Harano T. Examination of hemoglobin. In: Miwa S, editor. Miwa's Hematology. Tokyo: Bunkoudou; 2005. pp 1922-1933.
-
Hattori Y, Harano T. Examination of hemoglobin. In: Miwa S, editor. Miwa's Hematology. Tokyo: Bunkoudou; 2005. pp 1922-1933.
-
-
-
-
16
-
-
0015983097
-
Glycerol lysis time as a screening test for erythrocyte disorders
-
Gottfried EL, Robertson NA. Glycerol lysis time as a screening test for erythrocyte disorders. J Lab Clin Med 1974;83:323-333.
-
(1974)
J Lab Clin Med
, vol.83
, pp. 323-333
-
-
Gottfried, E.L.1
Robertson, N.A.2
-
17
-
-
0028075718
-
Evaluation of gene deletions by quantitative polymerase chain reaction. Experience with the α-thalassemia model
-
Borriello F, Weinberg DS, Mutter GL. Evaluation of gene deletions by quantitative polymerase chain reaction. Experience with the α-thalassemia model. Diagn Mol Pathol 1994;3:246-254.
-
(1994)
Diagn Mol Pathol
, vol.3
, pp. 246-254
-
-
Borriello, F.1
Weinberg, D.S.2
Mutter, G.L.3
-
18
-
-
0032843454
-
The precise breakpoints of a Filipino-type α-thalassemia-1 deletion found in two Japanese
-
Hattori Y, Okayama N, Ohba Y, et al. The precise breakpoints of a Filipino-type α-thalassemia-1 deletion found in two Japanese. Hemoglobin 1999;23:239-248.
-
(1999)
Hemoglobin
, vol.23
, pp. 239-248
-
-
Hattori, Y.1
Okayama, N.2
Ohba, Y.3
|