127 related articles for article (PubMed ID: 2408656)
21. 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
Blood; 1995 Feb; 85(4):1111-7. PubMed ID: 7531513
[TBL] [Abstract][Full Text] [Related]
22. Beta-globin gene haplotypes in the Saudi sickle cell anaemia patients.
el-Hazmi MA
Hum Hered; 1990; 40(3):177-86. PubMed ID: 1973147
[TBL] [Abstract][Full Text] [Related]
23. Elevated G gamma gene expression with specific beta S gene haplotype, normal gamma gene maps and presence of the Xmn I site -158 5' to the G gamma gene in Indian sickle cell anemia.
Lie-Injo LE; Lim ML; Randhawa Z; Vijayasilan T; Hassan K
Hemoglobin; 1987; 11(3):231-9. PubMed ID: 2443469
[TBL] [Abstract][Full Text] [Related]
24. 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
Blood; 1984 Nov; 64(5):1053-8. PubMed ID: 6207872
[TBL] [Abstract][Full Text] [Related]
25. Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms.
Wainscoat JS; Bell JI; Thein SL; Higgs DR; Sarjeant GR; Peto TE; Weatherall DJ
Mol Biol Med; 1983 Sep; 1(2):191-7. PubMed ID: 6094951
[TBL] [Abstract][Full Text] [Related]
26. Post-natal decline of fetal haemoglobin in homozygous sickle cell disease: relationship to parenteral Hb F levels.
Mason KP; Grandison Y; Hayes RJ; Serjeant BE; Serjeant GR; Vaidya S; Wood WG
Br J Haematol; 1982 Nov; 52(3):455-63. PubMed ID: 6181802
[TBL] [Abstract][Full Text] [Related]
27. Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patients.
Labie D; Pagnier J; Lapoumeroulie C; Rouabhi F; Dunda-Belkhodja O; Chardin P; Beldjord C; Wajcman H; Fabry ME; Nagel RL
Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2111-4. PubMed ID: 2580306
[TBL] [Abstract][Full Text] [Related]
28. 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
Blood; 1992 Aug; 80(3):816-24. PubMed ID: 1379090
[TBL] [Abstract][Full Text] [Related]
29. A gamma globin gene with G gamma-like promoter in a benin sickle cell anemia haplotype associated with elevated fetal hemoglobin.
Mishima N; Gilman JG; Huey LO; Milner PF
Prog Clin Biol Res; 1989; 316B():403-8. PubMed ID: 2482505
[No Abstract] [Full Text] [Related]
30. Analysis of high fetal hemoglobin production in sickle cell anemia patients from the Eastern Province of Saudi Arabia.
Miller BA; Salameh M; Ahmed M; Olivieri N; Huisman TH; Orkin SH; Nathan DG
Prog Clin Biol Res; 1987; 251():415-26. PubMed ID: 2448810
[No Abstract] [Full Text] [Related]
31. Sickle cell disease in Orissa State, India.
Kar BC; Satapathy RK; Kulozik AE; Kulozik M; Sirr S; Serjeant BE; Serjeant GR
Lancet; 1986 Nov; 2(8517):1198-201. PubMed ID: 2430154
[TBL] [Abstract][Full Text] [Related]
32. The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia.
Adekile A; Kutlar F; McKie K; Addington A; Elam D; Holley L; Clair B; Kutlar A
Eur J Haematol; 2005 Aug; 75(2):150-5. PubMed ID: 16004608
[TBL] [Abstract][Full Text] [Related]
33. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS.
Serjeant GR
Expert Rev Hematol; 2022 Feb; 15(2):107-116. PubMed ID: 35143361
[TBL] [Abstract][Full Text] [Related]
34. DNA haplotypes in Africans and West Indians with sickle cell anaemia or SC disease.
Konstantopoulos K; Vulliamy T; Swirsky D; Reeves JD; Kaeda J; Luzzatto L
Gene Geogr; 1996 Apr; 10(1):19-24. PubMed ID: 8913718
[TBL] [Abstract][Full Text] [Related]
35. Fetal Haemoglobin and β-globin Gene Cluster Haplotypes among Sickle Cell Patients in Chhattisgarh.
Bhagat S; Patra PK; Thakur AS
J Clin Diagn Res; 2013 Feb; 7(2):269-72. PubMed ID: 23542314
[TBL] [Abstract][Full Text] [Related]
36. Two independent genetic factors in the beta-globin gene cluster are associated with high G gamma-levels in the HbF of SS patients.
Gilman JG; Huisman TH
Blood; 1984 Aug; 64(2):452-7. PubMed ID: 6204701
[TBL] [Abstract][Full Text] [Related]
37. Two different forms of homozygous sickle cell disease occur in Saudi Arabia.
Padmos MA; Roberts GT; Sackey K; Kulozik A; Bail S; Morris JS; Serjeant BE; Serjeant GR
Br J Haematol; 1991 Sep; 79(1):93-8. PubMed ID: 1716963
[TBL] [Abstract][Full Text] [Related]
38. Ocular findings in Saudi Arabian patients with sickle cell disease.
al-Hazzaa S; Bird AC; Kulozik A; Serjeant BE; Serjeant GR; Thomas P; Padmos A
Br J Ophthalmol; 1995 May; 79(5):457-61. PubMed ID: 7612559
[TBL] [Abstract][Full Text] [Related]
39. Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.
Alsultan A; Alabdulaali MK; Griffin PJ; Alsuliman AM; Ghabbour HA; Sebastiani P; Albuali WH; Al-Ali AK; Chui DH; Steinberg MH
Br J Haematol; 2014 Feb; 164(4):597-604. PubMed ID: 24224700
[TBL] [Abstract][Full Text] [Related]
40. Relationship of haemoglobin F and alpha thalassaemia to severity of sickle-cell anaemia in the Eastern Province of Saudi Arabia.
Al-Awamy BH; Niazi GA; el-Mouzan MI; Altorki MT; Naeem MA
Ann Trop Paediatr; 1986 Dec; 6(4):261-5. PubMed ID: 2435232
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
