-
2
-
-
0004252202
-
-
Cambridge, UK: Cambridge University Press
-
Steinber MH, Forget BG, Higgs DR, Nagel RL. Disorders of Hemoglobin: Genetics, Pathopysiology and Clinical Management. Cambridge, UK: Cambridge University Press; 2001.
-
(2001)
Disorders of Hemoglobin: Genetics, Pathopysiology and Clinical Management
-
-
Steinber, M.H.1
Forget, B.G.2
Higgs, D.R.3
Nagel, R.L.4
-
3
-
-
0003154471
-
The thalassaemias
-
Stamatoyannopoulos G, Nienhuis AW, Majerus PH, Varmus H, eds. Philadelphia, Pa: W. B. Saunders
-
Weatherall SJ. The thalassaemias. In: Stamatoyannopoulos G, Nienhuis AW, Majerus PH, Varmus H, eds. The Molecular Bases of Blood Diseases. 2nd ed. Philadelphia, Pa: W. B. Saunders; 1994:157-205.
-
(1994)
The Molecular Bases of Blood Diseases. 2nd Ed.
, pp. 157-205
-
-
Weatherall, S.J.1
-
4
-
-
0032020108
-
The β and α-thalassemia repository
-
Huisman TH, Carver MF. The β and α-thalassemia repository. Hemoglobin. 1998;22(2):169-195.
-
(1998)
Hemoglobin
, vol.22
, Issue.2
, pp. 169-195
-
-
Huisman, T.H.1
Carver, M.F.2
-
5
-
-
0032416140
-
Pathophysiology of thalassaemia
-
Weatherall DJ. Pathophysiology of thalassaemia. Baillieres Clin Haematol. 1998;11(1):127-146.
-
(1998)
Baillieres Clin Haematol
, vol.11
, Issue.1
, pp. 127-146
-
-
Weatherall, D.J.1
-
6
-
-
0032429141
-
The Population Genetics of the haemoglobinopathies
-
Flint J, Harding RM, Boyce AJ, Clegg JB. The Population Genetics of the haemoglobinopathies. Baillieres Clin Haematol. 1998;11(1):1-51.
-
(1998)
Baillieres Clin Haematol
, vol.11
, Issue.1
, pp. 1-51
-
-
Flint, J.1
Harding, R.M.2
Boyce, A.J.3
Clegg, J.B.4
-
7
-
-
0024504090
-
β-thalassaemia mutations in Mediterranean populations
-
Cao A, Gossens M, Pirastu M. β-thalassaemia mutations in Mediterranean populations. Br J Haematol. 1989;71(3):309-312.
-
(1989)
Br J Haematol
, vol.71
, Issue.3
, pp. 309-312
-
-
Cao, A.1
Gossens, M.2
Pirastu, M.3
-
8
-
-
0242632723
-
The spectrum of β-thalassaemia mutations in the Arab populations
-
Zahed L. The spectrum of β-thalassaemia mutations in the Arab populations. J Biomed Biotechnol. 2001;1(3):129-132.
-
(2001)
J Biomed Biotechnol
, vol.1
, Issue.3
, pp. 129-132
-
-
Zahed, L.1
-
9
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215-1216.
-
(1988)
Nucleic Acids Res
, vol.16
, Issue.3
, pp. 1215-1216
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
10
-
-
0026948189
-
Detection of the most common mutations causing β-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS)
-
Fortina P, Dotti G, Conant R, et al. Detection of the most common mutations causing β-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS). PCR Methods Appl. 1992;2(2):163-166.
-
(1992)
PCR Methods Appl
, vol.2
, Issue.2
, pp. 163-166
-
-
Fortina, P.1
Dotti, G.2
Conant, R.3
-
11
-
-
0027449674
-
Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: Application to prenatal diagnosis in Sicily
-
Maggio A, Giambona A, Cai SP, Wall J, Kan YW, Chehab FF. Rapid and simultaneous typing of hemoglobin S, hemoglobin C, and seven Mediterranean beta-thalassemia mutations by covalent reverse dot-blot analysis: application to prenatal diagnosis in Sicily. Blood. 1993;81(1):239-242.
-
(1993)
Blood
, vol.81
, Issue.1
, pp. 239-242
-
-
Maggio, A.1
Giambona, A.2
Cai, S.P.3
Wall, J.4
Kan, Y.W.5
Chehab, F.F.6
-
12
-
-
0025470852
-
Frequencies of common beta-thalassaemia alleles among different populations: Variability in clinical severity
-
Huisman TH. Frequencies of common beta-thalassaemia alleles among different populations: variability in clinical severity. Br J Haematol. 1990;75(4):454-457.
-
(1990)
Br J Haematol
, vol.75
, Issue.4
, pp. 454-457
-
-
Huisman, T.H.1
-
13
-
-
0018907025
-
Sickle beta 0 thalassemia in the Eastern Saudi Arabia
-
Pembrey ME, Perrine RP, Wood WG, Weatherall DJ. Sickle beta 0 thalassemia in the Eastern Saudi Arabia. Am J Hum Genet. 1980;32(1):26-41.
-
(1980)
Am J Hum Genet
, vol.32
, Issue.1
, pp. 26-41
-
-
Pembrey, M.E.1
Perrine, R.P.2
Wood, W.G.3
Weatherall, D.J.4
-
14
-
-
0033232193
-
Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia
-
El-Hazmi MA, Warsy AS. Appraisal of sickle-cell and thalassaemia genes in Saudi Arabia. East Mediterr Health J. 1999;5(6):1147-1153.
-
(1999)
East Mediterr Health J
, vol.5
, Issue.6
, pp. 1147-1153
-
-
El-Hazmi, M.A.1
Warsy, A.S.2
-
15
-
-
0029117207
-
Molecular defects in beta-thalassaemias in the population of Saudi Arabia
-
El-Hazmi MA, Al-Swailem AR, Warsy AS. Molecular defects in beta-thalassaemias in the population of Saudi Arabia. Hum Hered. 1995;45(5):278-285.
-
(1995)
Hum Hered
, vol.45
, Issue.5
, pp. 278-285
-
-
El-Hazmi, M.A.1
Al-Swailem, A.R.2
Warsy, A.S.3
-
16
-
-
0029044446
-
Spectrum of beta-thalassaemia mutations in the population of Saudi Arabia
-
Hasounah FH, Sejeny SA, Omer JA, Old JM, Oliver RW. Spectrum of beta-thalassaemia mutations in the population of Saudi Arabia. Hum Hered. 1995;45(4):231-234.
-
(1995)
Hum Hered
, vol.45
, Issue.4
, pp. 231-234
-
-
Hasounah, F.H.1
Sejeny, S.A.2
Omer, J.A.3
Old, J.M.4
Oliver, R.W.5
-
17
-
-
0033429567
-
Identification and clinical presentation of beta thalassaemia mutations in the eastern region of Saudi Arabia
-
El-Harth EH, Kuhnau W, Schmidtke J, Stuhrmann M, Nasserallah Z, Al-Shahiri A. Identification and clinical presentation of beta thalassaemia mutations in the eastern region of Saudi Arabia. J Med Genet. 1999;36(12):935-937.
-
(1999)
J Med Genet
, vol.36
, Issue.12
, pp. 935-937
-
-
El-Harth, E.H.1
Kuhnau, W.2
Schmidtke, J.3
Stuhrmann, M.4
Nasserallah, Z.5
Al-Shahiri, A.6
-
18
-
-
0028641678
-
Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs
-
Adekile AD, Gu LH, Baysal E, et al. Molecular characterization of alpha-thalassemia determinants, beta-thalassemia alleles, and beta S haplotypes among Kuwaiti Arabs. Acta Haematol. 1994;92(4):176-181.
-
(1994)
Acta Haematol
, vol.92
, Issue.4
, pp. 176-181
-
-
Adekile, A.D.1
Gu, L.H.2
Baysal, E.3
-
19
-
-
0031873069
-
Molecular basis of β-thalassemia in Bahrain: An epicenter for a Middle East specific mutation
-
Jassim N, Merghoub T, Pascaud O, et al. Molecular basis of β-thalassemia in Bahrain: an epicenter for a Middle East specific mutation. Ann NY Acad Sci.1988;850:407-409.
-
(1988)
Ann NY Acad Sci
, vol.850
, pp. 407-409
-
-
Jassim, N.1
Merghoub, T.2
Pascaud, O.3
-
20
-
-
0027955750
-
The spectrum of β-thalassemia mutations in the UAE national population
-
Quaife R, Al-Gazali L, Abbes S, et al. The spectrum of β-thalassemia mutations in the UAE national population. J Med Genet. 1994;31(1):59-61.
-
(1994)
J Med Genet
, vol.31
, Issue.1
, pp. 59-61
-
-
Quaife, R.1
Al-Gazali, L.2
Abbes, S.3
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