These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
72 related articles for article (PubMed ID: 3489336)
1. Characterization of G6PD deficiency and thalassaemia in Papua New Guinea. Yenchitsomanus P; Summers KM; Chockkalingam C; Board PG P N G Med J; 1986 Mar; 29(1):53-8. PubMed ID: 3489336 [No Abstract] [Full Text] [Related]
2. 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]
3. Glucose-6-phosphate dehydrogenase deficiency in Papua New Guinea. The description of 13 new variants. Chockkalingam K; Board PG; Nurse GT Hum Genet; 1982; 60(2):189-92. PubMed ID: 7076260 [TBL] [Abstract][Full Text] [Related]
4. Do tribal communities show an inverse relationship between sickle cell disorders and glucose-6-phosphate dehydrogenase deficiency in malaria endemic areas of Central-Eastern India? Balgir RS Homo; 2006; 57(2):163-76. PubMed ID: 16603161 [TBL] [Abstract][Full Text] [Related]
5. [An adult woman with homozygotic beta-thalassemia and heterozygotic G6PD-deficiency]. Smals AG; Lustermans FA Ned Tijdschr Geneeskd; 1969 Feb; 113(7):290-8. PubMed ID: 5767928 [No Abstract] [Full Text] [Related]
6. A new glucose 6 phosphate dehydrogenase variant G6PD Sinnai (34 G-->T). Mutations in brief no. 156. Online. Galanello R; Loi D; Sollaino C; Dessì S; Cao A; Melis MA Hum Mutat; 1998; 12(1):72-3. PubMed ID: 10627140 [TBL] [Abstract][Full Text] [Related]
7. Glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Ok Tedi impact region of Papua New Guinea. Schuurkamp GJ; Bhatia KK; Kereu RK; Bulungol PK Hum Biol; 1989 Jun; 61(3):387-406. PubMed ID: 2807263 [TBL] [Abstract][Full Text] [Related]
8. Patterns of sickle cell, thalassaemia and glucose-6-phosphate dehydrogenase deficiency genes in north-western Saudi Arabia. El-Hazmi MA; Jabbar FA; Al-Faleh FZ; Al-Swailem AR; Warsy AS Hum Hered; 1991; 41(1):26-34. PubMed ID: 2050379 [TBL] [Abstract][Full Text] [Related]
9. Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews. Karimi M; Yavarian M; Afrasiabi A; Dehbozorgian J; Rachmilewitz E Arch Med Res; 2008 Feb; 39(2):212-4. PubMed ID: 18164966 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. The role of the G6PD AEth376G/968C allele in glucose-6-phosphate dehydrogenase deficiency in the seerer population of Senegal. De Araujo C; Migot-Nabias F; Guitard J; Pelleau S; Vulliamy T; Ducrocq R Haematologica; 2006 Feb; 91(2):262-3. PubMed ID: 16461316 [TBL] [Abstract][Full Text] [Related]
13. Red cell genetic abnormalities and environmental interactions: a study in Tehamat Aseer. el-Hazmi MA J Trop Med Hyg; 1987 Apr; 90(2):61-7. PubMed ID: 3560299 [TBL] [Abstract][Full Text] [Related]
14. Study of glucose-6-phosphate dehydrogenase (G6PD) in the Kissan tribals of Orissa and the Kannikar tribals of Kerala, India. Devi ST; Saran SK; Nair G Anthropol Anz; 1993 Jun; 51(2):179-81. PubMed ID: 8333738 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. [Association of a triple genetic erythrocyte defect: thalassemia, sickle cell disease and glucose-6-phosphate dehydrogenase deficiency in a child of Calabro-Sardinian origin]. Sansone G; Vallarino G; Centa A Haematologica; 1967; 52(6):479-92. PubMed ID: 4976069 [No Abstract] [Full Text] [Related]
17. [The preliminary study on the gene mutations of sixty patients with G6PD deficiency in Yunnan province]. Yang Z; Chu J; Xu S; Lin K; Tao Y; Shi L Zhonghua Xue Ye Xue Za Zhi; 2000 Oct; 21(10):509-11. PubMed ID: 11877026 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Molecular analysis of glucose-6-dehydrogenase deficiency in Spain]. Vives Corrons JL; Zarza R; Aymerich JM; Boixadera J; Carrera A; Colomer D; Corbella M; Castro M; Crespo JM; Del Arco A; Erkiaga S; Font L; González I; Juncá J; Lausin A; Manrubia E; Martín Núñez G; Murga MJ; Oliva E; Pérez de Mendiguren B; Pujades MA; Remacha A; Rovira A; Villegas A Sangre (Barc); 1997 Oct; 42(5):391-8. PubMed ID: 9424740 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]