-
1
-
-
0024340685
-
Detection of β-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique
-
Winichagoon P, Kownkon J, Yenchitsomanus P, Thonglairoam V, Siritanaratku N, Fucharoen S: Detection of β-thalassemia and hemoglobin E genes in Thai by a DNA amplification technique. Hum Genet 1989;82:389-390.
-
(1989)
Hum Genet
, vol.82
, pp. 389-390
-
-
Winichagoon, P.1
Kownkon, J.2
Yenchitsomanus, P.3
Thonglairoam, V.4
Siritanaratku, N.5
Fucharoen, S.6
-
2
-
-
0032011557
-
1c as an indicator for the presence of Hb AE phenotype in diabetic-patients
-
1c as an indicator for the presence of Hb AE phenotype in diabetic-patients. Clin Chem 1998;44:660-662.
-
(1998)
Clin Chem
, vol.44
, pp. 660-662
-
-
Wong, S.C.1
Aw, T.C.2
-
3
-
-
0020049449
-
Construction of human gene libraries from small amounts of peripheral blood: Analysis of β-like globin genes
-
Ponez M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S: Construction of human gene libraries from small amounts of peripheral blood: Analysis of β-like globin genes. Hemoglobin 1982;6:27-36.
-
(1982)
Hemoglobin
, vol.6
, pp. 27-36
-
-
Ponez, M.1
Solowiejczyk, D.2
Harpel, B.3
Mory, Y.4
Schwartz, E.5
Surrey, S.6
-
4
-
-
0018304922
-
Hemoglobin E trait reexamined: A cause of microcytosis and erythrocytosis
-
Fairbanks VF, Gilchrist GS, Brimhall B, Jereb JA, Goldston ES: Hemoglobin E trait reexamined: A cause of microcytosis and erythrocytosis. Blood 1979;53:109-115.
-
(1979)
Blood
, vol.53
, pp. 109-115
-
-
Fairbanks, V.F.1
Gilchrist, G.S.2
Brimhall, B.3
Jereb, J.A.4
Goldston, E.S.5
-
5
-
-
0019969721
-
Hemoglobin E diseases: Hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for α-thalassemia
-
Wong SC, Ali MAM: Hemoglobin E diseases: Hematological, analytical, and biosynthetic studies in homozygotes and double heterozygotes for α-thalassemia. Am J Hematol 1982; 13:15-21.
-
(1982)
Am J Hematol
, vol.13
, pp. 15-21
-
-
Wong, S.C.1
Ali, M.A.M.2
-
6
-
-
0342713134
-
The coexistence of the genes for hemoglobin E and β-thalassemia in Thais, with resultant suppression of hemoglobin E synthesis
-
Tuchinda S, Rucknagcl DL, Minnich V, Boonyaprakob Y, Blankura K, Suvatee V: The coexistence of the genes for hemoglobin E and β-thalassemia in Thais, with resultant suppression of hemoglobin E synthesis. Am J Hum Genet 1964;16:311-335.
-
(1964)
Am J Hum Genet
, vol.16
, pp. 311-335
-
-
Tuchinda, S.1
Rucknagcl, D.L.2
Minnich, V.3
Boonyaprakob, Y.4
Blankura, K.5
Suvatee, V.6
-
7
-
-
0015135427
-
Double heterozygosity for hemoglobin E and hemoglobin New York in a Thai family
-
Pootrakul S, Wasi S, Na-Nakorn S, Dixon GH: Double heterozygosity for hemoglobin E and hemoglobin New York in a Thai family. J Med Assoc Thai 1971;54:688-697.
-
(1971)
J Med Assoc Thai
, vol.54
, pp. 688-697
-
-
Pootrakul, S.1
Wasi, S.2
Na-Nakorn, S.3
Dixon, G.H.4
-
8
-
-
0017337111
-
Interaction of haemoglobin E with α-thalassemia and haemoglobin constant spring
-
Ganesan J, Lie-Injo LE, Ng TS, George R: Interaction of haemoglobin E with α-thalassemia and haemoglobin Constant Spring. Acta Haematol 1977;57:109-115.
-
(1977)
Acta Haematol
, vol.57
, pp. 109-115
-
-
Ganesan, J.1
Lie-Injo, L.E.2
Ng, T.S.3
George, R.4
-
9
-
-
0343147649
-
Identification of hemoglobin E by the isopropanol solubility test
-
Ali MAM, Quinlan A, Wong SC: Identification of hemoglobin E by the isopropanol solubility test. Clin Chem 1980;13:148-150.
-
(1980)
Clin Chem
, vol.13
, pp. 148-150
-
-
Ali, M.A.M.1
Quinlan, A.2
Wong, S.C.3
-
11
-
-
0019940070
-
'Silent' β-thalassacmia caused by a 'silent' β-chain mutant: The pathogenesis of a syndrome of thalassacmia intermedia
-
Fessas Ph, Loukopoulos D, Loutradi-Anagnostouy A, Komis G: 'Silent' β-thalassacmia caused by a 'silent' β-chain mutant: The pathogenesis of a syndrome of thalassacmia intermedia. Br J Haematol 1982;51:577-583.
-
(1982)
Br J Haematol
, vol.51
, pp. 577-583
-
-
Fessas, Ph.1
Loukopoulos, D.2
Loutradi-Anagnostouy, A.3
Komis, G.4
-
14
-
-
0031782419
-
Hemoglobin E β-thalassemia: An increasingly common disease with some diagnostic pitfalls
-
Weatherall DJ: Hemoglobin E β-thalassemia: An increasingly common disease with some diagnostic pitfalls. J Pediatr 1998;132:765-767.
-
(1998)
J Pediatr
, vol.132
, pp. 765-767
-
-
Weatherall, D.J.1
-
16
-
-
0027408741
-
Severity differences in β-thalassacmia/haemoglobin E syndromes: Implication of genetic factors
-
Winichagoon P, Thonglairoam V, Fucharoen S, Wilairat P, Fukumaki Y, Wasi P: Severity differences in β-thalassacmia/haemoglobin E syndromes: Implication of genetic factors. Br J Haematol 1993;83:633-639.
-
(1993)
Br J Haematol
, vol.83
, pp. 633-639
-
-
Winichagoon, P.1
Thonglairoam, V.2
Fucharoen, S.3
Wilairat, P.4
Fukumaki, Y.5
Wasi, P.6
|