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Molecular and Cellular Biology|August 1, 1987
Expression of the affected A gamma globin gene associated with Greek nondeletion hereditary persistence of fetal hemoglobinC J Stoeckert, J E Metherall, M Yamakawa, et al.
The Journal of Biological Chemistry|August 15, 1991
A splice site mutation of the beta-spectrin gene causing exon skipping in hereditary elliptocytosis associated with a truncated beta-spectrin chainP G Gallagher, W T Tse, F Costa, et al.
Blood|October 1, 1993
Poikilocytic hereditary elliptocytosis associated with spectrin Alexandria: an alpha I/50b Kd variant that is caused by a single amino acid deletionP G Gallagher, W E Roberts, L Benoit, et al.
Experimental Hematology|March 1, 1992
A structurally abnormal erythropoietin receptor gene in a human erythroleukemia cell lineJ C Ward, K W Harris, L A Penny, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Assignment of the gene for beta-spectrin (SPTB) to chromosome 14q23----q24.2 by in situ hybridizationY Fukushima, M G Byers, P C Watkins, et al.
Blood|November 1, 1984
Lactoferrin biosynthesis during granulocytopoiesisT A Rado, J Bollekens, G St Laurent, et al.
Genomics|February 1, 1997
Organization of the human protein 4.1 genomic locus: new insights into the tissue-specific alternative splicing of the pre-mRNAF Baklouti, S C Huang, T J Vulliamy, et al.
Cell Biology International Reports|May 1, 1977
Gene mapping by fluorescent in situ hybridizationS W Cheung, P V Tishler, L Atkins, et al.
British Journal of Haematology|October 1, 1994
Location and PCR-based detection of three polymorphisms of the human erythrocyte beta-spectrin gene (SPTB)P G Gallagher, M C Lecomte, C Galand, et al.
Blood|September 1, 1991
Heterogeneity of the molecular basis of hereditary pyropoikilocytosis and hereditary elliptocytosis associated with increased levels of the spectrin alpha I/74-kilodalton tryptic peptideP B Floyd, P G Gallagher, L A Valentino, et al.
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