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Journal Abstract Search
343 related items for PubMed ID: 16910233
1. Co-inheritance of alpha and beta-thalassemia in a Jordanian family. Al Qaddoumi AA. Clin Lab Sci; 2006; 19(3):165-8. PubMed ID: 16910233 [Abstract] [Full Text] [Related]
6. Coinheritance of the different copy numbers of alpha-globin gene modifies severity of beta-thalassemia/Hb E disease. Sripichai O, Munkongdee T, Kumkhaek C, Svasti S, Winichagoon P, Fucharoen S. Ann Hematol; 2008 May; 87(5):375-9. PubMed ID: 18026953 [Abstract] [Full Text] [Related]
7. A complex haemoglobinopathy diagnosis in a family with both beta zero- and alpha (zero/+)-thalassaemia homozygosity. Giordano PC, Harteveld CL, Bok LA, van Delft P, Batelaan D, Beemer FA, Bernini LF. Eur J Hum Genet; 1999 May; 7(2):163-8. PubMed ID: 10196699 [Abstract] [Full Text] [Related]
9. [Current views of thalassemia intermedia]. Longinotti M, Dore F, Oggiano L, Pardini S, Pistidda P, Guiso L, Frogheri L, Bonfigli S, Murineddu M, Rimini E. Recenti Prog Med; 1992 Apr; 83(4):233-40. PubMed ID: 1626119 [Abstract] [Full Text] [Related]
10. Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará. De Lemos Cardoso G, Guerreiro JF. Am J Hum Biol; 2010 Apr; 22(5):573-7. PubMed ID: 20737602 [Abstract] [Full Text] [Related]
13. The clinical significance of the spectrum of interactions of CAP+1 (A-->C), a silent beta-globin gene mutation, with other beta-thalassemia mutations and globin gene modifiers in north Indians. Garewal G, Das R, Awasthi A, Ahluwalia J, Marwaha RK. Eur J Haematol; 2007 Nov; 79(5):417-21. PubMed ID: 17900295 [Abstract] [Full Text] [Related]
18. Frequency of positive XmnIGgamma polymorphism and coinheritance of common alpha thalassemia mutations do not show statistically significant difference between thalassemia major and intermedia cases with homozygous IVSII-1 mutation. Neishabury M, Azarkeivan A, Najmabadi H. Blood Cells Mol Dis; 2010 Dec; 44(2):95-9. PubMed ID: 19892574 [Abstract] [Full Text] [Related]