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2. Screening for abnormal hemoglobins: who, when, and how. McCurdy PR Prim Care; 1980 Sep; 7(3):451-60. PubMed ID: 6905205 [TBL] [Abstract][Full Text] [Related]
3. Methods for detection of beta-thalassemia trait for sickle cell screening programs. Honig GR; Hoversten GH Am J Med Technol; 1974 Dec; 40(12):523-8. PubMed ID: 4440708 [No Abstract] [Full Text] [Related]
4. The role of a sickle cell center in comprehensive screening and counseling for sickle cell and related disorders. Lutcher CL; Huisman TH; Dorsey WM; Mayson S; Ludvigsen B; Smith AT South Med J; 1974 Mar; 67(3):259-64. PubMed ID: 4814171 [No Abstract] [Full Text] [Related]
5. Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene. Steinberg MH; Embury SH Birth Defects Orig Artic Ser; 1987; 23(5A):43-8. PubMed ID: 3689929 [No Abstract] [Full Text] [Related]
6. The genetics of sickle cell anemia and related syndromes. Rucknagel DL Arch Intern Med; 1974 Apr; 133(4):595-606. PubMed ID: 4594396 [No Abstract] [Full Text] [Related]
7. Perspectives in sickle cell disease screening. O'Brien RT South Med J; 1974 Nov; 67(11):1269-71. PubMed ID: 4428208 [No Abstract] [Full Text] [Related]
8. Sickle cell-Hb Lepore Boston syndrome. Uncommon differential diagnosis to homozygous sickle cell disease. Stevens MC; Lehmann H; Mason KP; Serjeant BE; Serjeant GR Am J Dis Child; 1982 Jan; 136(1):19-22. PubMed ID: 7055103 [TBL] [Abstract][Full Text] [Related]
9. Screening for sickle cell disease. Gaston M South Med J; 1974 Mar; 67(3):257-8. PubMed ID: 4814170 [No Abstract] [Full Text] [Related]
10. Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait. Shaeffer JR; DeSimone J; Kleve LJ Biochem Genet; 1975 Dec; 13(11-12):783-8. PubMed ID: 1200978 [TBL] [Abstract][Full Text] [Related]
11. A rare case of a compound heterozygote hemoglobin S/hemoglobin Fannin-Lubbock-I individual. Is it a sickling disorder? Burns NK; Risin SA Lab Hematol; 2010 Jun; 16(2):26-7. PubMed ID: 20534428 [No Abstract] [Full Text] [Related]
13. Laboratory Diagnosis of sickling hemoglobinopathies. Steinberg MH; Adams JG South Med J; 1978 Apr; 71(4):413-6. PubMed ID: 635620 [TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of sickle-cell anemia and alpha G Philadelphia. Study of a Fetus also at risk for H b S/beta+-thalassemia. Alter BP; Friedman S; Hobbins JC; Mahoney MJ; Sherman AS; McSweeney JF; Nathan DG; Schwartz E N Engl J Med; 1976 May; 294(19):1040-1. PubMed ID: 3736 [No Abstract] [Full Text] [Related]
18. Sickle solubility test to screen for sickle cell trait: what's the harm? Tubman VN; Field JJ Hematology Am Soc Hematol Educ Program; 2015; 2015():433-5. PubMed ID: 26637754 [No Abstract] [Full Text] [Related]
19. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait. Steinberg MH; Coleman MB; Adams JG; Hartmann RC; Saba H; Anagnou NP Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832 [TBL] [Abstract][Full Text] [Related]
20. Hemoglobin Setif and in vitro pseudosickling noted in a family with co-existent alpha and beta thalassemia. Raik E; Powell E; Fleming P; Gordon S Pathology; 1983 Oct; 15(4):453-6. PubMed ID: 6674875 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]