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2. What determines severity in sickle-cell disease? Schechter AN; Bunn HF N Engl J Med; 1982 Feb; 306(5):295-7. PubMed ID: 6172711 [No Abstract] [Full Text] [Related]
3. 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]
5. [Haemoglobin S/beta thalassaemia in a Greek family: a case study (author's transl)]. Fischer M; Hopmeier P; Lurf M; Neuwald C; Lachmann D Wien Klin Wochenschr; 1979 Jan; 91(2):45-8. PubMed ID: 433279 [TBL] [Abstract][Full Text] [Related]
6. Molecular biology of hemoglobin: its application to sickle cell anemia and thalassemia. Kan YW Schweiz Med Wochenschr Suppl; 1991; 43():51-4. PubMed ID: 1726857 [TBL] [Abstract][Full Text] [Related]
7. Characterization of hemoglobin variants. Prenatal diagnosis on a fetus at risk of having the hemoglobin variants S and/or C in combination with beta-thalassemia. Blanke S Scand J Clin Lab Invest Suppl; 1989; 194():51-5. PubMed ID: 2772555 [TBL] [Abstract][Full Text] [Related]
10. [Hemoglobinosis SC ("African rheumatism") and the hemoglobin C heterozygous carrier state]. Kononiachenko VA; Troitskaia OV; Iushkova NM; Iudina LI Probl Gematol Pereliv Krovi; 1979 Nov; 24(11):20-4. PubMed ID: 504093 [No Abstract] [Full Text] [Related]
11. 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]
12. [Treatment of thalassemia and sickle cell anemia in children]. Girot R Ann Pediatr (Paris); 1978; 25(5-6):277-84. PubMed ID: 16114336 [No Abstract] [Full Text] [Related]