-
2
-
-
0016691182
-
Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural loci
-
Kan YW, Dozy AM, Varmus HE, et al. Deletion of α-globin genes in haemoglobin-H disease demonstrates multiple α-globin structural loci. Nature 1975; 255: 255-56.
-
(1975)
Nature
, vol.255
, pp. 255-256
-
-
Kan, Y.W.1
Dozy, A.M.2
Varmus, H.E.3
-
4
-
-
0001916646
-
Molecular mechanisms of alpha thalassaemia
-
Steinberg, MH, Forget, BG, Higgs, DR, Nagel, RL (eds). Cambridge: Cambridge University Press
-
Higgs DR. Molecular mechanisms of alpha thalassaemia. In: Steinberg, MH, Forget, BG, Higgs, DR, Nagel, RL (eds), Disorders of Haemoglobin: Genetics, Pathophysiology, and Clinical Management, 1st ed. Cambridge: Cambridge University Press, 2001; 17: 405-30.
-
(2001)
Disorders of Haemoglobin: Genetics, Pathophysiology, and Clinical Management, 1st Ed.
, vol.17
, pp. 405-430
-
-
Higgs, D.R.1
-
5
-
-
33646803415
-
Abnormal human haemoglobins. Haemoglobin 'Bart's': A foetal haemoglobin without a chains
-
Hunt JA, and Lehman H. Abnormal human haemoglobins. Haemoglobin 'Bart's': a foetal haemoglobin without a chains. Nature 1959; 184: 872-73.
-
(1959)
Nature
, vol.184
, pp. 872-873
-
-
Hunt, J.A.1
Lehman, H.2
-
6
-
-
0031053941
-
Molecular defects in Hb H hydrops foetalis
-
Chan V Chan VW, Tang M, Lau K, Todd D, Chan TK. Molecular defects in Hb H hydrops foetalis. Br J Haematol 1997; 96: 224-28.
-
(1997)
Br J Haematol
, vol.96
, pp. 224-228
-
-
Chan, V.1
Chan, V.W.2
Tang, M.3
Lau, K.4
Todd, D.5
Chan, T.K.6
-
7
-
-
0014746252
-
The haemoglobin constitution of infants with the haemoglobin Bart's hydrops foetalis syndrome
-
Weatherall DJ, Clegg JB, Boon WH. The haemoglobin constitution of infants with the haemoglobin Bart's hydrops foetalis syndrome. Br J Haematol 1970; 18: 357-67.
-
(1970)
Br J Haematol
, vol.18
, pp. 357-367
-
-
Weatherall, D.J.1
Clegg, J.B.2
Boon, W.H.3
-
8
-
-
0025805963
-
Molecular characterization of severe alpha-thalassaemia causing hydrops fetalis in Taiwan
-
Ko TM, Hsieh FJ, Hsu PM, Lee TY. Molecular characterization of severe alpha-thalassaemia causing hydrops fetalis in Taiwan. Am J Med Genet 1991; 39: 317-20.
-
(1991)
Am J Med Genet
, vol.39
, pp. 317-320
-
-
Ko, T.M.1
Hsieh, F.J.2
Hsu, P.M.3
Lee, T.Y.4
-
11
-
-
0021807743
-
Homozygous α-thalassaemia: Clinical presentation, diagnosis and management. A review of 46 cases
-
Liang ST, Wong VC, So WW, Ma HK, Chan V and Todd D. Homozygous α-thalassaemia: clinical presentation, diagnosis and management. A review of 46 cases. Br J Obstet Gynaecol 1985; 92: 680-84.
-
(1985)
Br J Obstet Gynaecol
, vol.92
, pp. 680-684
-
-
Liang, S.T.1
Wong, V.C.2
So, W.W.3
Ma, H.K.4
Chan, V.5
Todd, D.6
-
12
-
-
0029913489
-
Human α-Thalassaemia Syndrome: Detection of Molecular Defects
-
Kattamis AC, Camaschella C, Sivera P, Surrey S, Fortina P. Human α-Thalassaemia Syndrome: Detection of Molecular Defects. Am J Hematol 1996; 53: 81-91.
-
(1996)
Am J Hematol
, vol.53
, pp. 81-91
-
-
Kattamis, A.C.1
Camaschella, C.2
Sivera, P.3
Surrey, S.4
Fortina, P.5
-
14
-
-
30344471937
-
Antenatal diagnosis for alpha-thalassaemia in Malaysia - A four-year review from 1996 - 2000
-
Tan JAMA, Wee YC, Tan KL, Wong YC, Chow WPT, Yap SF. Antenatal diagnosis for alpha-thalassaemia in Malaysia - a four-year review from 1996 - 2000. IMR J 2000; 4: 73-77.
-
(2000)
IMR J
, vol.4
, pp. 73-77
-
-
Tan, J.A.M.A.1
Wee, Y.C.2
Tan, K.L.3
Wong, Y.C.4
Chow, W.P.T.5
Yap, S.F.6
-
15
-
-
0038523501
-
-
Thalassaemia Diagnostic Service (ThalDS). Kuala Lumpur: SP-Muda Printing Sdn Bhd
-
George E. Thalassaemia carrier diagnosis in Malaysia. Thalassaemia Diagnostic Service (ThalDS). Kuala Lumpur: SP-Muda Printing Sdn Bhd, 1998.
-
(1998)
Thalassaemia Carrier Diagnosis in Malaysia
-
-
George, E.1
-
17
-
-
0020363734
-
The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene
-
Proudfoot NJ, Gil A, Maniatis T. The structure of the human zeta-globin gene and a closely linked, nearly identical pseudogene. Cell 1982; 31: 553-63.
-
(1982)
Cell
, vol.31
, pp. 553-563
-
-
Proudfoot, N.J.1
Gil, A.2
Maniatis, T.3
-
18
-
-
0023663725
-
Detection of sickle cell anaemia and thalassaemias
-
Chehab FF, Doherty M, Cai SP, Kan YW, Cooper S, Rubin, EM. Detection of sickle cell anaemia and thalassaemias. Nature 1987; 329: 293-94.
-
(1987)
Nature
, vol.329
, pp. 293-294
-
-
Chehab, F.F.1
Doherty, M.2
Cai, S.P.3
Kan, Y.W.4
Cooper, S.5
Rubin, E.M.6
-
19
-
-
0033025838
-
A reverse dot-blot method for rapid detection of non-deletion alpha thalassaemia
-
Chan V, Yam I, Chen FE, Chan TK. A reverse dot-blot method for rapid detection of non-deletion alpha thalassaemia. Br J Haematol 1999; 104: 513-15.
-
(1999)
Br J Haematol
, vol.104
, pp. 513-515
-
-
Chan, V.1
Yam, I.2
Chen, F.E.3
Chan, T.K.4
-
20
-
-
0035728091
-
Detection of severe nondeletional alpha-thalassaemia mutations using a single-tube multiplex ARMS assay
-
Eng B, Patterson M, Walker L, Chui DH, Waye JS. Detection of severe nondeletional alpha-thalassaemia mutations using a single-tube multiplex ARMS assay. Genet Test 2001; 5: 327-29.
-
(2001)
Genet Test
, vol.5
, pp. 327-329
-
-
Eng, B.1
Patterson, M.2
Walker, L.3
Chui, D.H.4
Waye, J.S.5
-
21
-
-
0035412399
-
A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassaemia
-
Tan, AS, Quah, TC, Low, PS, Chong, SS. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for alpha-thalassaemia. Blood 2001; 98: 250-51.
-
(2001)
Blood
, vol.98
, pp. 250-251
-
-
Tan, A.S.1
Quah, T.C.2
Low, P.S.3
Chong, S.S.4
-
22
-
-
0034091983
-
Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions
-
Liu YT, Old JM, Miles K, Fisher CA, Weatherall DJ, Clegg JB. Rapid detection of alpha-thalassaemia deletions and alpha-globin gene triplication by multiplex polymerase chain reactions. Br J Haematol 2000; 108: 295-99.
-
(2000)
Br J Haematol
, vol.108
, pp. 295-299
-
-
Liu, Y.T.1
Old, J.M.2
Miles, K.3
Fisher, C.A.4
Weatherall, D.J.5
Clegg, J.B.6
|