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Journal Abstract Search
164 related items for PubMed ID: 2329681
21. Alpha thalassaemia in American blacks: a study of a family with five cases of haemoglobin H disease. Bellevue R, Dosik H, Rieder RF. Br J Haematol; 1979 Feb; 41(2):193-202. PubMed ID: 427029 [Abstract] [Full Text] [Related]
22. A molecular marker associated with mild hemoglobin H disease. George E, Ferguson V, Yakas J, Kronenberg H, Trent RJ. Pathology; 1989 Jan; 21(1):27-30. PubMed ID: 2762043 [Abstract] [Full Text] [Related]
24. Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype. Galanello R, Paglietti E, Melis MA, Giagu L, Cao A. Acta Haematol; 1984 Jan; 72(1):34-6. PubMed ID: 6089487 [Abstract] [Full Text] [Related]
27. Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes. Di Rienzo A, Novelletto A, Aliquò MC, Bianco I, Tagarelli A, Brancati C, Colombo B, Felicetti L. Am J Hum Genet; 1986 Nov; 39(5):631-9. PubMed ID: 2878610 [Abstract] [Full Text] [Related]
29. 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 Nov; 7(2):163-8. PubMed ID: 10196699 [Abstract] [Full Text] [Related]
31. A report of 8 cases with hemoglobin H disease in an Iranian family. Azarkeivan A, Neishabury M, Hadavi V, Esteghamat F, Enrahimkhani S, Najmabadi H. Pediatr Hematol Oncol; 2010 Aug; 27(5):405-12. PubMed ID: 20670167 [Abstract] [Full Text] [Related]
32. A 6-year-old girl with hemoglobin H disease. Ueda T, Migita M, Yamanishi M, Maeda M, Harano K, Fukunaga Y. J Nippon Med Sch; 2011 Aug; 78(2):101-4. PubMed ID: 21551967 [Abstract] [Full Text] [Related]