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The Journal of Clinical Investigation|January 15, 1997
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemiaP G Gallagher, M J Petruzzi, S A Weed, et al.
The Journal of Clinical Investigation|March 1, 1995
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin geneP G Gallagher, S A Weed, W T Tse, et al.
Blood|August 1, 1992
Spectrin Jendouba: an alpha II/31 spectrin variant that is associated with elliptocytosis and carries a mutation distant from the dimer self-association siteN Alloisio, R Wilmotte, L Morlé, et al.
Cancer|July 1, 1990
Results of neoadjuvant chemotherapy and radiation therapy in the breast-conserving treatment of 250 patients with all stages of infiltrative breast cancerC Jacquillat, M Weil, F Baillet, et al.
Anais Da Academia Brasileira De Ciencias|January 11, 2001
Cytogenetic damage related to low levels of methyl mercury contamination in the Brazilian AmazonM I Amorim, D Mergler, M O Bahia, et al.
The Journal of Biological Chemistry|April 10, 1980
Nucleotide sequence of the coding portion of human alpha globin messenger RNAJ T Wilson, L B Wilson, V B Reddy, et al.
The Journal of Clinical Investigation|August 1, 1990
Two elliptocytogenic alpha I/74 variants of the spectrin alpha I domain. Spectrin Culoz (GGT----GTT; alpha I 40 Gly----Val) and spectrin Lyon (CTT----TTT; alpha I 43 Leu---Phe)L Morlé, A F Roux, N Alloisio, et al.
The Journal of Clinical Investigation|October 1, 1989
Sequence and exon-intron organization of the DNA encoding the alpha I domain of human spectrin. Application to the study of mutations causing hereditary elliptocytosisK E Sahr, T Tobe, A Scarpa, et al.
Blood|July 1, 1987
A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicingG F Atweh, C Wong, R Reed, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1979
RNA polymerase III transcriptional units are interspersed among human non-alpha-globin genesC Duncan, P A Biro, P V Choudary, et al.
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