179 related articles for article (PubMed ID: 4045955)
1. Survey on haemoglobin variants, beta thalassaemia, glucose-6-phosphate dehydrogenase deficiency, and haptoglobin types in Turks from western Thrace.
Aksoy M; Kutlar A; Kutlar F; Dinçol G; Erdem S; Baştesbihçi S
J Med Genet; 1985 Aug; 22(4):288-90. PubMed ID: 4045955
[TBL] [Abstract][Full Text] [Related]
2. Survey on haemoglobin variants, beta-thalassaemia, glucose-6-phosphate dehydrogenase deficiency and haptoglobin types in Turkish people living in Manavgat, Serik and Boztepe (Antalya).
Aksoy M; Dinçol G; Erdem S
Hum Hered; 1980; 30(1):3-6. PubMed ID: 7353885
[TBL] [Abstract][Full Text] [Related]
3. Red cell genetic abnormalities in Peninsular Arabs: sickle haemoglobin, G6PD deficiency, and alpha and beta thalassaemia.
White JM; Byrne M; Richards R; Buchanan T; Katsoulis E; Weerasingh K
J Med Genet; 1986 Jun; 23(3):245-51. PubMed ID: 3723553
[TBL] [Abstract][Full Text] [Related]
4. Haemoglobin variants, beta-thalassaemia and G-6-PD types in Liberia.
Willcox MC; Beckman L
Hum Hered; 1981; 31(6):339-47. PubMed ID: 7333623
[TBL] [Abstract][Full Text] [Related]
5. The burden and consequences of inherited blood disorders among young children in western Kenya.
Suchdev PS; Ruth LJ; Earley M; Macharia A; Williams TN
Matern Child Nutr; 2014 Jan; 10(1):135-44. PubMed ID: 22973867
[TBL] [Abstract][Full Text] [Related]
6. Glucose-6-phosphate dehydrogenase deficiency, thalassaemia & abnormal haemoglobins in Bohra Muslims.
Jain RC; Chhaparwal JK; Bansal G; Gupta RK
Indian J Med Res; 1984 Jun; 79():789-91. PubMed ID: 6519703
[No Abstract] [Full Text] [Related]
7. Malaria and human polymorphisms.
Livincstone FB
Annu Rev Genet; 1971; 5():33-64. PubMed ID: 16097650
[No Abstract] [Full Text] [Related]
8. Frequency of haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in Basra.
Hassan MK; Taha JY; Al-Naama LM; Widad NM; Jasim SN
East Mediterr Health J; 2003; 9(1-2):45-54. PubMed ID: 15562732
[TBL] [Abstract][Full Text] [Related]
9. Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies.
Samuel AP; Saha N; Acquaye JK; Omer A; Ganeshaguru K; Hassounh E
Hum Hered; 1986; 36(2):107-12. PubMed ID: 3699836
[TBL] [Abstract][Full Text] [Related]
10. Hemoglobin variants in India.
Ajmani M; Sharma A; Talukder G
Acta Genet Med Gemellol (Roma); 1978; 27():11-29. PubMed ID: 751379
[TBL] [Abstract][Full Text] [Related]
11. Student screening for inherited blood disorders in Bahrain.
Al-Arrayed S; Hafadh N; Amin S; Al-Mukhareq H; Sanad H
East Mediterr Health J; 2003 May; 9(3):344-52. PubMed ID: 15751927
[TBL] [Abstract][Full Text] [Related]
12. Inherited anaemias in the Greek community of Cape Town.
Bonafede RP; Botha MC; Beighton P
J Med Genet; 1979 Jun; 16(3):197-200. PubMed ID: 469897
[TBL] [Abstract][Full Text] [Related]
13. Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.
Horányi M; Szelényi J; Rona G; Lang A; Lehmann H; Hollán SR
Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):654-60. PubMed ID: 6162733
[TBL] [Abstract][Full Text] [Related]
14. Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.
Badens C; Martinez di Montemuros F; Thuret I; Michel G; Mattei JF; Cappellini MD; Lena-Russo D
Hematol J; 2000; 1(4):264-8. PubMed ID: 11920200
[TBL] [Abstract][Full Text] [Related]
15. Interaction between the glucose-6-phosphate dehydrogenase deficiency and thalassaemia genes at phenotype level.
Sanna G; Frau F; Melis MA; Galanello R; De Virgiliis S; Cao A
Br J Haematol; 1980 Apr; 44(4):555-61. PubMed ID: 7378315
[TBL] [Abstract][Full Text] [Related]
16. Sickle cell hemoglobin, beta-thalassemia and G6PD deficiency in tribes of Maharashtra, India.
Rao VR; Gorakshakar AC
Gene Geogr; 1990 Dec; 4(3):131-4. PubMed ID: 2129613
[TBL] [Abstract][Full Text] [Related]
17. Falciparum malaria and beta-thalassaemia trait in northern Liberia.
Willcox M; Björkman A; Brohult J
Ann Trop Med Parasitol; 1983 Aug; 77(4):335-47. PubMed ID: 6357119
[TBL] [Abstract][Full Text] [Related]
18. Genetic Blood Disorders Survey in the Sultanate of Oman.
Al-Riyami A; Ebrahim GJ
J Trop Pediatr; 2003 Jul; 49 Suppl 1():i1-20. PubMed ID: 12934793
[TBL] [Abstract][Full Text] [Related]
19. Haemoglobin gene frequencies in the Jamaican population: a study in 100,000 newborns.
Serjeant GR; Serjeant BE; Forbes M; Hayes RJ; Higgs DR; Lehmann H
Br J Haematol; 1986 Oct; 64(2):253-62. PubMed ID: 3778823
[TBL] [Abstract][Full Text] [Related]
20. Abnormal haemoglobins in the Sudan savanna of Nigeria. I. Prevalence of haemoglobins and relationships between sickle cell trait, malaria and survival.
Fleming AF; Storey J; Molineaux L; Iroko EA; Attai ED
Ann Trop Med Parasitol; 1979 Apr; 73(2):161-72. PubMed ID: 315211
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]