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7. [Ethnogeographical characteristics of the distribution of hereditary erythrocytopathies among the population of the Fergana Valley]. Saliev KK Gematol Transfuziol; 1986 Nov; 31(11):7-10. PubMed ID: 2948870 [No Abstract] [Full Text] [Related]
9. [Hereditary hemolytic anemias]. Busch D Med Klin; 1970 Mar; 65(10):432-6. PubMed ID: 5419577 [No Abstract] [Full Text] [Related]
10. 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]
11. Studies on four hereditary blood disorders in Iceland. Jensson O Acta Med Scand Suppl; 1978; 618():1-28. PubMed ID: 308294 [No Abstract] [Full Text] [Related]
12. 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]
14. Hereditary elliptocytosis (the first report in Thailand) in association with erythrocyte glucose-6-phosphate dehydrogenase deficiency and hemoglobin E. Panich V; Na-Nakorn S; Wasi P J Med Assoc Thai; 1970 Aug; 53(8):593-600. PubMed ID: 5506338 [No Abstract] [Full Text] [Related]
15. Molecular genetics of hereditary elliptocytosis and hereditary spherocytosis. Delaunay J; Alloisio N; Morle L; Baklouti F; Dalla Venezia N; Maillet P; Wilmotte R Ann Genet; 1996; 39(4):209-21. PubMed ID: 9037349 [TBL] [Abstract][Full Text] [Related]
16. Inherited disorders in the Afrikaner population of southern Africa. Part II. Skeletal, dermal and haematological conditions; the Afrikaners of Gamkaskloof; demographic considerations. Botha MC; Beighton P S Afr Med J; 1983 Oct; 64(17):664-7. PubMed ID: 6414096 [TBL] [Abstract][Full Text] [Related]
17. A biochemical study in anemic children in Iran. Daneshbod G Acta Med Iran; 1974 Dec; 17(3-4):141-7. PubMed ID: 4534328 [No Abstract] [Full Text] [Related]
18. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes. Miwa S; Fujii H Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052 [TBL] [Abstract][Full Text] [Related]
19. Disorders of red cell membrane. An X; Mohandas N Br J Haematol; 2008 May; 141(3):367-75. PubMed ID: 18341630 [TBL] [Abstract][Full Text] [Related]