Thein SL - Search Results

1

Lamin B-receptor mutations in Pelger-Huët anomaly.

Best S, Salvati F, Kallo J, Garner C, Height S, Thein SL, Rees DC. Best S, et al. Among authors: thein sl. Br J Haematol. 2003 Nov;123(3):542-4. doi: 10.1046/j.1365-2141.2003.04621.x. Br J Haematol. 2003. PMID: 14617022 Free article.

2

The spectrum of beta thalassaemia in Burma.

Brown JM, Thein SL, Weatherall DJ, Mar KM. Brown JM, et al. Among authors: thein sl. Br J Haematol. 1992 Aug;81(4):574-8. doi: 10.1111/j.1365-2141.1992.tb02994.x. Br J Haematol. 1992. PMID: 1356413

3

Molecular characterization of a novel 10.3 kb deletion causing beta-thalassaemia with unusually high Hb A2.

Craig JE, Kelly SJ, Barnetson R, Thein SL. Craig JE, et al. Among authors: thein sl. Br J Haematol. 1992 Dec;82(4):735-44. doi: 10.1111/j.1365-2141.1992.tb06952.x. Br J Haematol. 1992. PMID: 1482661

4

Hemoglobin Chesterfield (beta 28 Leu----Arg) produces the phenotype of inclusion body beta thalassemia.

Thein SL, Best S, Sharpe J, Paul B, Clark DJ, Brown MJ. Thein SL, et al. Blood. 1991 Jun 15;77(12):2791-3. Blood. 1991. PMID: 1675132 Free article. No abstract available.

5

A novel delta 0 mutation in cis with Hb Knossos: a study of different genetic interactions in three Egyptian families.

Olds RJ, Sura T, Jackson B, Wonke B, Hoffbrand AV, Thein SL. Olds RJ, et al. Among authors: thein sl. Br J Haematol. 1991 Jul;78(3):430-6. doi: 10.1111/j.1365-2141.1991.tb04460.x. Br J Haematol. 1991. PMID: 1873227

6

A simple and rapid method of direct sequencing using Dynabeads.

Thein SL, Hinton J. Thein SL, et al. Br J Haematol. 1991 Sep;79(1):113-5. doi: 10.1111/j.1365-2141.1991.tb08016.x. Br J Haematol. 1991. PMID: 1911367 No abstract available.

7

The molecular basis of HPFH in a British family identified by heteroduplex formation.

Craig JE, Sheerin SM, Barnetson R, Thein SL. Craig JE, et al. Among authors: thein sl. Br J Haematol. 1993 May;84(1):106-10. doi: 10.1111/j.1365-2141.1993.tb03032.x. Br J Haematol. 1993. PMID: 7687855

8

A base substitution (T-->C) in codon 29 of the alpha 2-globin gene causes alpha thalassaemia.

Hall GW, Thein SL, Newland AC, Chisholm M, Traeger-Synodinos J, Kanavakis E, Kattamis C, Higgs DR. Hall GW, et al. Among authors: thein sl. Br J Haematol. 1993 Nov;85(3):546-52. doi: 10.1111/j.1365-2141.1993.tb03346.x. Br J Haematol. 1993. PMID: 8136277

9

Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies.

Ho PJ, Rochette J, Rees DC, Fisher CA, Huehns ER, Will AM, Thein SL. Ho PJ, et al. Among authors: thein sl. Hemoglobin. 1996 May;20(2):103-12. doi: 10.3109/03630269609027915. Hemoglobin. 1996. PMID: 8811313

10

Interaction of hemoglobin E and pyrimidine 5' nucleotidase deficiency.

Rees DC, Duley J, Simmonds HA, Wonke B, Thein SL, Clegg JB, Weatherall DJ. Rees DC, et al. Among authors: thein sl. Blood. 1996 Oct 1;88(7):2761-7. Blood. 1996. PMID: 8839873 Free article.

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