-
1
-
-
0034605653
-
Single gene disorders or complex traits: Lessons from the thalassaemias and other monogenic diseases
-
Weatherall DJ. Single gene disorders or complex traits: Lessons from the thalassaemias and other monogenic diseases. BMJ 2000;321:1117-1120.
-
(2000)
BMJ
, vol.321
, pp. 1117-1120
-
-
Weatherall, D.J.1
-
2
-
-
0034321997
-
Genetic factors affecting clinical severity in beta-thalassemia syndromes
-
Winichagoon P, Fucharoen S, Chen P, et al. Genetic factors affecting clinical severity in beta-thalassemia syndromes. J Pediatr Hematol Oncol 2000;22:573-580.
-
(2000)
J Pediatr Hematol Oncol
, vol.22
, pp. 573-580
-
-
Winichagoon, P.1
Fucharoen, S.2
Chen, P.3
-
3
-
-
0024692852
-
Incidence study of heterozygous [beta]-thalassemia in northern Taiwan
-
Ko TM, Hsu PM, Chen CJ, et al. Incidence study of heterozygous [beta]-thalassemia in northern Taiwan. J Formos Med Assoc 1989;88:678-681.
-
(1989)
J Formos Med Assoc
, vol.88
, pp. 678-681
-
-
Ko, T.M.1
Hsu, P.M.2
Chen, C.J.3
-
4
-
-
0043179035
-
The incidence of [beta]-thalassemia trait in Taiwan
-
Lin KH, Lin LL, Su S, et al. The incidence of [beta]-thalassemia trait in Taiwan. Int J Pediatr Hematol Oncol 1994;1:383-388.
-
(1994)
Int J Pediatr Hematol Oncol
, vol.1
, pp. 383-388
-
-
Lin, K.H.1
Lin, L.L.2
Su, S.3
-
6
-
-
0030058529
-
Current status of thalassemia and the sickle cell syndromes in Greece
-
Loukopoulos D. Current status of thalassemia and the sickle cell syndromes in Greece. Semin Hematol 1996;33:76-86.
-
(1996)
Semin Hematol
, vol.33
, pp. 76-86
-
-
Loukopoulos, D.1
-
7
-
-
0019363539
-
Prevention of thalassaemia in Cyprus
-
Angastiniotis MA, Hadjiminas MG. Prevention of thalassaemia in Cyprus. Lancet 1981;1:369-371.
-
(1981)
Lancet
, vol.1
, pp. 369-371
-
-
Angastiniotis, M.A.1
Hadjiminas, M.G.2
-
8
-
-
0031886857
-
Molecular study and prenatal diagnosis of [alpha]- and [beta]- thalassemia in Chinese
-
Ko TM, Xu X. Molecular study and prenatal diagnosis of [alpha]- and [beta]- thalassemia in Chinese. J Formos Med Assoc 1998;97:5-15.
-
(1998)
J Formos Med Assoc
, vol.97
, pp. 5-15
-
-
Ko, T.M.1
Xu, X.2
-
9
-
-
0031972656
-
Beta-thalassaemia intermedia: Is it possible consistently to predict phenotype from genotype?
-
Ho PJ, Hall GW, Luo LY, et al. Beta-thalassaemia intermedia: Is it possible consistently to predict phenotype from genotype? Br J Haematol 1998;100:70-78.
-
(1998)
Br J Haematol
, vol.100
, pp. 70-78
-
-
Ho, P.J.1
Hall, G.W.2
Luo, L.Y.3
-
10
-
-
0141642025
-
Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC
-
Su YN, Lee CN, Hung CC, et al. Rapid detection of beta-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC. Hum Mutat 2003;22:326-336.
-
(2003)
Hum Mutat
, vol.22
, pp. 326-336
-
-
Su, Y.N.1
Lee, C.N.2
Hung, C.C.3
-
12
-
-
0023957711
-
Cord blood screening for alpha-thalassemia in northern Taiwan
-
Ko TM, Hsieh FJ, Chen CJ, et al. Cord blood screening for alpha-thalassemia in northern Taiwan. J Formos Med Asso 1988;87:146-149.
-
(1988)
J Formos Med Asso
, vol.87
, pp. 146-149
-
-
Ko, T.M.1
Hsieh, F.J.2
Chen, C.J.3
-
13
-
-
0026795743
-
Results of therapy for beta-thalassemia major
-
Lin KH, Lin KS. Results of therapy for beta-thalassemia major. J Formos Med Assoc 1992;91:126-130.
-
(1992)
J Formos Med Assoc
, vol.91
, pp. 126-130
-
-
Lin, K.H.1
Lin, K.S.2
-
14
-
-
0033536288
-
The beta-thalassemias
-
Olivieri NF. The beta-thalassemias. N Engl J Med 1999;341:99-109.
-
(1999)
N Engl J Med
, vol.341
, pp. 99-109
-
-
Olivieri, N.F.1
-
15
-
-
0034690731
-
A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports
-
Streetly A. A national screening policy for sickle cell disease and thalassaemia major for the United Kingdom. Questions are left after two evidence based reports. BMJ 2000;320:1353-1354.
-
(2000)
BMJ
, vol.320
, pp. 1353-1354
-
-
Streetly, A.1
-
16
-
-
0032554535
-
Coordinated neonatal screening programme for haemoglobin disorders is needed
-
Streetly A, Maxwell K, Campbell B. Coordinated neonatal screening programme for haemoglobin disorders is needed. BMJ 1998;316:937.
-
(1998)
BMJ
, vol.316
, pp. 937
-
-
Streetly, A.1
Maxwell, K.2
Campbell, B.3
-
17
-
-
0031004892
-
Molecular characterization of beta-thalassemia in Taiwan and the identification of two new mutations
-
Ko TM, Tseng LH, Hsu PM, et al. Molecular characterization of beta-thalassemia in Taiwan and the identification of two new mutations. Hemoglobin 1997;21;131-142.
-
(1997)
Hemoglobin
, vol.21
, pp. 131-142
-
-
Ko, T.M.1
Tseng, L.H.2
Hsu, P.M.3
-
19
-
-
0034606928
-
Informed choice in genetic screening for thalassaemia during pregnancy: Audit from a national confidential inquiry
-
Modell B, Harris R, Lane B, et al. Informed choice in genetic screening for thalassaemia during pregnancy: Audit from a national confidential inquiry. BMJ 2000;320:337-341.
-
(2000)
BMJ
, vol.320
, pp. 337-341
-
-
Modell, B.1
Harris, R.2
Lane, B.3
-
20
-
-
0025751692
-
How well do we manage families with genetic problems? A national confidential enquiry into counseling for genetic disorders should tell us
-
Harris R. How well do we manage families with genetic problems? A national confidential enquiry into counseling for genetic disorders should tell us. BMJ 1991;303:1412-1413.
-
(1991)
BMJ
, vol.303
, pp. 1412-1413
-
-
Harris, R.1
-
21
-
-
0035171882
-
A national register for surveillance of inherited disorders: Beta thalassaemia in the United Kingdom
-
Modell B, Khan M, Darlison M, et al. A national register for surveillance of inherited disorders: Beta thalassaemia in the United Kingdom. Bull World Health Organ 2001;79:1006-1013.
-
(2001)
Bull World Health Organ
, vol.79
, pp. 1006-1013
-
-
Modell, B.1
Khan, M.2
Darlison, M.3
-
22
-
-
0032547570
-
A multidisciplinary approach for improving services in primary care: Randomised controlled trial of screening for haemoglobin disorders
-
Modell M, Wonke B, Anionwu E, et al. A multidisciplinary approach for improving services in primary care: Randomised controlled trial of screening for haemoglobin disorders. BMJ 1998;317:788-791.
-
(1998)
BMJ
, vol.317
, pp. 788-791
-
-
Modell, M.1
Wonke, B.2
Anionwu, E.3
|