Serjeant G - Search Results

1

Fetal hemoglobin levels in sickle cell disease and normal individuals are partially controlled by an X-linked gene located at Xp22.2.

Dover GJ, Smith KD, Chang YC, Purvis S, Mays A, Meyers DA, Sheils C, Serjeant G. Dover GJ, et al. Among authors: serjeant g. Blood. 1992 Aug 1;80(3):816-24. Blood. 1992. PMID: 1379090 Free article.

2

The cellular basis for different fetal hemoglobin levels among sickle cell individuals with two, three, and four alpha-globin genes.

Dover GJ, Chang VT, Boyer SH, Serjeant GR, Antonarakis S, Higgs DR. Dover GJ, et al. Among authors: serjeant gr. Blood. 1987 Jan;69(1):341-4. Blood. 1987. PMID: 2431731 Free article.

3

Production of F cells in sickle cell anemia: regulation by a genetic locus or loci separate from the beta-globin gene cluster.

Boyer SH, Dover GJ, Serjeant GR, Smith KD, Antonarakis SE, Embury SH, Margolet L, Noyes AN, Boyer ML, Bias WB. Boyer SH, et al. Among authors: serjeant gr. Blood. 1984 Nov;64(5):1053-8. Blood. 1984. PMID: 6207872 Free article.

4

An analysis of fetal hemoglobin variation in sickle cell disease: the relative contributions of the X-linked factor, beta-globin haplotypes, alpha-globin gene number, gender, and age.

Chang YC, Smith KD, Moore RD, Serjeant GR, Dover GJ. Chang YC, et al. Among authors: serjeant gr. Blood. 1995 Feb 15;85(4):1111-7. Blood. 1995. PMID: 7531513 Free article.

5

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions.

Economou EP, Antonarakis SE, Kazazian HH Jr, Serjeant GR, Dover GJ. Economou EP, et al. Among authors: serjeant gr. Blood. 1991 Jan 1;77(1):174-7. Blood. 1991. PMID: 1702028 Free article.

6

Factors affecting prepubertal growth in homozygous sickle cell disease.

Singhal A, Morris J, Thomas P, Dover G, Higgs D, Serjeant G. Singhal A, et al. Among authors: serjeant g. Arch Dis Child. 1996 Jun;74(6):502-6. doi: 10.1136/adc.74.6.502. Arch Dis Child. 1996. PMID: 8758125 Free PMC article.

7

Alpha thalassemia changes erythrocyte heterogeneity in sickle cell disease.

Noguchi CT, Dover GJ, Rodgers GP, Serjeant GR, Antonarakis SE, Anagnou NP, Higgs DR, Weatherall DJ, Schechter AN. Noguchi CT, et al. Among authors: serjeant gr. J Clin Invest. 1985 May;75(5):1632-7. doi: 10.1172/JCI111870. J Clin Invest. 1985. PMID: 2581999 Free PMC article.

8

Are there clinical phenotypes of homozygous sickle cell disease?

Alexander N, Higgs D, Dover G, Serjeant GR. Alexander N, et al. Among authors: serjeant gr. Br J Haematol. 2004 Aug;126(4):606-11. doi: 10.1111/j.1365-2141.2004.05025.x. Br J Haematol. 2004. PMID: 15287956 Free article.

9

Fetal hemoglobin levels and beta (s) globin haplotypes in an Indian populations with sickle cell disease.

Kulozik AE, Kar BC, Satapathy RK, Serjeant BE, Serjeant GR, Weatherall DJ. Kulozik AE, et al. Among authors: serjeant gr, serjeant be. Blood. 1987 Jun;69(6):1742-6. Blood. 1987. PMID: 2437982 Free article.

10

Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both.

Antonarakis SE, Boehm CD, Serjeant GR, Theisen CE, Dover GJ, Kazazian HH Jr. Antonarakis SE, et al. Among authors: serjeant gr. Proc Natl Acad Sci U S A. 1984 Feb;81(3):853-6. doi: 10.1073/pnas.81.3.853. Proc Natl Acad Sci U S A. 1984. PMID: 6583683 Free PMC article.

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