-
2
-
-
0037305250
-
Hemoglobin H disease: Not necessarily a benign disorder
-
DOI 10.1182/blood-2002-07-1975
-
Chui DH, Fucharoen S, Chan V. Hemoglobin H disease: not necessarily a benign disorder. Blood. 2003;101:791-800. (Pubitemid 36139341)
-
(2003)
Blood
, vol.101
, Issue.3
, pp. 791-800
-
-
Chui, D.H.K.1
Fucharoen, S.2
Chan, V.3
-
4
-
-
0023728783
-
Isoelectric focusing for measurement of hemoglobin Barts levels in cord blood and detection of á thalassemia
-
Das S, Vashit K, Segal S, et al. Isoelectric focusing for measurement of hemoglobin Barts levels in cord blood and detection of á thalassemia. Indian J Med Res. 1988;87:62-66.
-
(1988)
Indian J Med Res
, vol.87
, pp. 62-66
-
-
Das, S.1
Vashit, K.2
Segal, S.3
-
5
-
-
0029970758
-
Alpha genotyping in a heterogeneous Indian population [10]
-
DOI 10.1002/(SICI)1096-8652(199610)53:2<149::AID-AJH22>3.0.CO;2-9
-
Nadkarni A, Gorakshakar A, Mohanty D, et al. Alpha genotyping in a heterogeneous Indian population [letter]. Am J Hematol. 1996;53:149-150. (Pubitemid 26377712)
-
(1996)
American Journal of Hematology
, vol.53
, Issue.2
, pp. 149-150
-
-
Nadkarni, A.H.1
Gorakshakar, A.C.2
Mohanty, D.3
Colah, R.B.4
-
6
-
-
0026551487
-
Combination of three different forms of α thalassemia in a large Indian family from Durban, South Africa: Hematological observations
-
Fei Y, Liu JC, Jogessar VB, et al. Combination of three different forms of α thalassemia in a large Indian family from Durban, South Africa: hematological observations. Acta Haematol. 1992;87:11-15.
-
(1992)
Acta Haematol
, vol.87
, pp. 11-15
-
-
Fei, Y.1
Liu, J.C.2
Jogessar, V.B.3
-
7
-
-
0025969406
-
Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, India
-
Fodde R, Harteveld CL, Losekoot M, et al. Multiple recombination events are responsible for the heterogeneity of alpha(+)-thalassemia haplotypes among the forest tribes of Andhra Pradesh, India. Ann Hum Genet. 1991;55(pt 1):43-50.
-
(1991)
Ann Hum Genet
, vol.55
, Issue.PART 1
, pp. 43-50
-
-
Fodde, R.1
Harteveld, C.L.2
Losekoot, M.3
-
8
-
-
0026233475
-
High prevalence and heterogeneity of thalassemias in Orissa
-
Misra RC, Ram B, Mohapatra BC, et al. High prevalence and heterogeneity of thalassemias in Orissa. Indian J Med Res. 1999;94:391-394.
-
(1999)
Indian J Med Res
, vol.94
, pp. 391-394
-
-
Misra, R.C.1
Ram, B.2
Mohapatra, B.C.3
-
9
-
-
0030811674
-
Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth?
-
Desai S, Colah R, Gupte S, et al. Is cellulose acetate electrophoresis a suitable technique for detection of Hb Bart's at birth? Hum Hered. 1997;47:181-184. (Pubitemid 27309565)
-
(1997)
Human Heredity
, vol.47
, Issue.4
, pp. 181-184
-
-
Desai, S.1
Colah, R.2
Gupte, S.3
Mohanty, D.4
-
10
-
-
77951181341
-
Investigation of abnormal haemoglobins and thalassaemia
-
Lewis SM, Bain BJ, Bates I, eds. 10th ed. New York, NY: Churchill Livingstone
-
Wild B, Bain BJ. Investigation of abnormal haemoglobins and thalassaemia. In: Lewis SM, Bain BJ, Bates I, eds. Dacie and Lewis Practical Haematology. 10th ed. New York, NY: Churchill Livingstone; 2006:271-310.
-
(2006)
Dacie and Lewis Practical Haematology
, pp. 271-310
-
-
Wild, B.1
Bain, B.J.2
-
11
-
-
0348110520
-
Determination of the breakpoint and molecular diagnosis of a common alpha-thalassaemia- 1 deletion in the Indian population
-
Shaji RV, Eunice SE, Badya S, et al. Determination of the breakpoint and molecular diagnosis of a common alpha-thalassaemia- 1 deletion in the Indian population. Br J Haematol. 2003;123:942-947.
-
(2003)
Br J Haematol
, vol.123
, pp. 942-947
-
-
Shaji, R.V.1
Eunice, S.E.2
Badya, S.3
-
13
-
-
0034492252
-
Phenotypic and molecular diversity of haemoglobin H disease: A Greek experience
-
DOI 10.1046/j.1365-2141.2000.02448.x
-
Kanavakis E, Papassotiriou I, Karagiorga M, et al. Phenotypic and molecular diversity of haemoglobin H disease: a Greek experience. Br J Haematol. 2000;111:915-923. (Pubitemid 32098932)
-
(2000)
British Journal of Haematology
, vol.111
, Issue.3
, pp. 915-923
-
-
Kanavakis, E.1
Papassotiriou, I.2
Karagiorga, M.3
Vrettou, C.4
Metaxotou-Mavrommati, A.5
Stamoulakatou, A.6
Kattamis, C.7
Traeger-Synodinos, J.8
-
14
-
-
0028875253
-
The instability of the membrane skeleton in thalassemic red blood cells
-
Yuan J, Bunyaratvej A, Fucharoen S, et al. The instability of the membrane skeleton in thalassemic red blood cells. Blood. 1995;86:3945-3950.
-
(1995)
Blood
, vol.86
, pp. 3945-3950
-
-
Yuan, J.1
Bunyaratvej, A.2
Fucharoen, S.3
-
16
-
-
45549092191
-
Prevalence and molecular characterization of α-thalassemia syndromes among Indians
-
DOI 10.1089/gte.2007.0080
-
Nadkarni A, Phanasgaonkar S, Colah R, et al. Prevalence and molecular characterization of α-thalassemia syndromes among Indians. Genet Test. 2008;12:177-180. (Pubitemid 351860435)
-
(2008)
Genetic Testing
, vol.12
, Issue.2
, pp. 177-180
-
-
Nadkarni, A.1
Phanasgaonkar, S.2
Colah, R.3
Mohanty, D.4
Ghosh, K.5
-
17
-
-
0028838819
-
A new á-chain variant Hb Sallanches [α2 104(G11)Cys → Tyr] associated with HbH disease in one homozygous patient
-
Morlé F, Francina A, Ducroq R, et al. A new á-chain variant Hb Sallanches [α2 104(G11)Cys → Tyr] associated with HbH disease in one homozygous patient. Br J Haematol. 1995;91:608-611.
-
(1995)
Br J Haematol
, vol.91
, pp. 608-611
-
-
Morlé, F.1
Francina, A.2
Ducroq, R.3
-
18
-
-
0033708636
-
Homozygous Hb Sallanches [α104(G11) Cys → Tyr] in a Pakistani child with HbH disease
-
Waye J, Walker L, Chui DHK, et al. Homozygous Hb Sallanches [α104(G11) Cys → Tyr] in a Pakistani child with HbH disease. Hemoglobin. 2000;24:355-357.
-
(2000)
Hemoglobin
, vol.24
, pp. 355-357
-
-
Waye, J.1
Walker, L.2
Chui, D.H.K.3
-
19
-
-
33746268977
-
Hb Sallanches [α104(G11)Cys → Tyr, TGCTAC]: An unstable hemoglobin variant found in an Indian child
-
Dash S, Harano K, Menon S. Hb Sallanches [α104(G11)Cys → Tyr, TGCTAC]: an unstable hemoglobin variant found in an Indian child. Hemoglobin. 2006;30:393-396.
-
(2006)
Hemoglobin
, vol.30
, pp. 393-396
-
-
Dash, S.1
Harano, K.2
Menon, S.3
-
20
-
-
47949117716
-
Unstable and thalassemic α-chain hemoglobin variants: A cause of HbH disease and thalassemia intermedia
-
Wacjman H, Traeger-Synodinos J, Papassotiriou L, et al. Unstable and thalassemic α-chain hemoglobin variants: a cause of HbH disease and thalassemia intermedia. Hemoglobin. 2008;32:327-349.
-
(2008)
Hemoglobin
, vol.32
, pp. 327-349
-
-
Wacjman, H.1
Traeger-Synodinos, J.2
Papassotiriou, L.3
-
21
-
-
34547798065
-
A laboratory strategy for genotyping hemoglobin H disease in the Chinese
-
Chan AY, So CK, Ma ES, et al. A laboratory strategy for genotyping hemoglobin H disease in the Chinese. J Clin Pathol. 2007;60:1-5.
-
(2007)
J Clin Pathol
, vol.60
, pp. 1-5
-
-
Chan, A.Y.1
So, C.K.2
Ma, E.S.3
|