-
1
-
-
0003550379
-
The thalassemia syndromes
-
Blackwell Scientific London, Oxford
-
Weatherall DJ, Clegg JB (1981) The thalassemia syndromes. Blackwell Scientific London, Oxford
-
(1981)
-
-
Weatherall, D.J.1
Clegg, J.B.2
-
2
-
-
0003739602
-
Hemoglobin: Molecular, genetic, and clinical aspect
-
WB Saunders, Philadelphia
-
Bun HF, Forget BG (1986) Hemoglobin: molecular, genetic, and clinical aspect. WB Saunders, Philadelphia
-
(1986)
-
-
Bun, H.F.1
Forget, B.G.2
-
3
-
-
0029334707
-
Molecular diagnosis of thalassemia in Taiwan
-
Chang JG, Liu HJ (1995) Molecular diagnosis of thalassemia in Taiwan. Kaohsiung J Med Sci 11:371-378
-
(1995)
Kaohsiung J. Med. Sci.
, vol.11
, pp. 371-378
-
-
Chang, J.G.1
Liu, H.J.2
-
4
-
-
0031886857
-
Molecular study and prenatal diagnosis of alpha-and beta-thalassemias in Chinese
-
Ko TM, Xu X (1998) Molecular study and prenatal diagnosis of alpha-and beta-thalassemias in Chinese. J Formos Med Assoc 97:5-15
-
(1998)
J. Formos. Med. Assoc.
, vol.97
, pp. 5-15
-
-
Ko, T.M.1
Xu, X.2
-
6
-
-
0033536288
-
The beta-thalassemias
-
Oliveri NF (1999) The beta-thalassemias. N Engl J Med 341:99-109
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 99-109
-
-
Oliveri, N.F.1
-
7
-
-
0026788309
-
Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites
-
Chang JG, Chen PH, Chiou SS, et al. (1992) Rapid diagnosis of beta-thalassemia mutations in Chinese by naturally and amplified created restriction sites. Blood 80:2092-2096
-
(1992)
Blood
, vol.80
, pp. 2092-2096
-
-
Chang, J.G.1
Chen, P.H.2
Chiou, S.S.3
-
8
-
-
0022432381
-
0 thalassemia deletion: Comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints
-
0 thalassemia deletion: comparison to other deletions in the human β-globin gene cluster and sequence analysis of the breakpoints. Nucleic Acids Res 13:6559-6575
-
(1985)
Nucleic Acids Res.
, vol.13
, pp. 6559-6575
-
-
Mager, D.L.1
Henthorn, P.S.2
Smithies, O.3
-
9
-
-
0022271874
-
0-thalassemia: Three types observed in South-Chinese families
-
0-thalassemia: three types observed in South-Chinese families. Blood 66:1430-1435
-
(1985)
Blood
, vol.66
, pp. 1430-1435
-
-
Zeng, Y.T.1
Huang, S.Z.2
Chen, B.3
Chen, B.4
Liang, A.M.5
Chang, T.6
Harano, T.7
Huisman, T.H.J.8
-
10
-
-
0027497960
-
0-thalassemia deletion in a Chinese families
-
0-thalassemia deletion in a Chinese families. Blood 81:1624-1629
-
(1993)
Blood
, vol.81
, pp. 1624-1629
-
-
Zhang, J.W.1
Song, W.F.2
Zhao, Y.J.3
Wu, G.Y.4
Qiu, Z.M.5
Wang, F.N.6
Chen, S.S.7
Stamatoyannopoulos, G.8
-
11
-
-
0033784895
-
Molecular characterization and PCR detection of a deletional HPFH: Application to rapid prenatal diagnosis for compound heterozygotes of this defect with β-thalassemia in a Chinese family
-
Xu XM, Li ZO, Liu ZY, Zhong XL, Zhao YZ, Mo QH (2000) Molecular characterization and PCR detection of a deletional HPFH: application to rapid prenatal diagnosis for compound heterozygotes of this defect with β-thalassemia in a Chinese family. Am J Hematol 65:183-188
-
(2000)
Am. J. Hematol.
, vol.65
, pp. 183-188
-
-
Xu, X.M.1
Li, Z.O.2
Liu, Z.Y.3
Zhong, X.L.4
Zhao, Y.Z.5
Mo, Q.H.6
-
12
-
-
0031689498
-
0-thalassemia deletion lies in an L1 family sequence: Implications for the mechanism of deletion and the reactivation of the Gγ-globin gene
-
0-thalassemia deletion lies in an L1 family sequence: implications for the mechanism of deletion and the reactivation of the Gγ-globin gene. Hum Genet 103:90-95
-
(1998)
Hum. Genet.
, vol.103
, pp. 90-95
-
-
Zhang, X.Q.1
Zhang, J.W.2
-
13
-
-
0028214609
-
Rapid detection of deletions causing δβ thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification
-
Craig JE, Barnetson RA, Prior J, Raven JL, Thein SL (1994) Rapid detection of deletions causing δβ thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification. Blood 83:1673-1682
-
(1994)
Blood
, vol.83
, pp. 1673-1682
-
-
Craig, J.E.1
Barnetson, R.A.2
Prior, J.3
Raven, J.L.4
Thein, S.L.5
-
14
-
-
0031871713
-
Molecular basis of hereditary persistence of fetal hemoglobin
-
Forget BG (1998) Molecular basis of hereditary persistence of fetal hemoglobin. Ann N Y Acad Sci 850:38-44
-
(1998)
Ann. N Y Acad. Sci.
, vol.850
, pp. 38-44
-
-
Forget, B.G.1
-
15
-
-
0038638765
-
The δ- and β-thalassemia repository
-
Baysal E, Carver MFH (1998) The δ- and β-thalassemia repository. Hemoglobin 22:292-298
-
(1998)
Hemoglobin
, vol.22
, pp. 292-298
-
-
Baysal, E.1
Carver, M.F.H.2
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