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Experimental Hematology|July 25, 2000
Gene transfer to ankyrin-deficient bone marrow corrects spherocytosis in vitroG J Dooner, J E Barker, P G Gallagher, et al.Gene|January 1, 1985
Polyadenylation of a human mitochondrial ribosomal RNA transcript detected by molecular cloningS J Baserga, A J Linnenbach, S Malcolm, et al.Human Genetics|October 1, 1990
Evidence that expression of Sp alpha I/65 hereditary elliptocytosis is compounded by a genetic factor that is linked to the homologous alpha-spectrin alleleD Guetarni, A F Roux, N Alloisio, et al.Blood|December 1, 1984
Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black populationF S Collins, C D Boehm, P G Waber, et al.American Journal of Hematology|March 1, 1997
Ankyrin Bugey: a de novo deletional frameshift variant in exon 6 of the ankyrin gene associated with spherocytosisL Morlé, M Bozon, N Alloisio, et al.JAMA|April 13, 1979
Prenatal diagnosis of homozygous alpha-thalassemiaA M Dozy, E N Forman, D N Abuelo, et al.Neurotoxicology|January 1, 1996
Evidence of early nervous system dysfunction in Amazonian populations exposed to low-levels of methylmercuryJ Lebel, D Mergler, M Lucotte, et al.Blood|September 1, 1994
Developmental regulation of human gamma- and beta-globin genes in the absence of the locus control regionJ Starck, R Sarkar, M Romana, et al.Annals of the New York Academy of Sciences|January 1, 1990
Expression of human globin genes in transgenic mice carrying the beta-globin gene cluster with a mutation causing G gamma beta + hereditary persistence of fetal hemoglobinM Tanaka, J A Nolan, A K Bhargava, et al.Blood|August 1, 1989
Spectrin Tunis (Sp alpha I/78), an elliptocytogenic variant, is due to the CGG----TGG codon change (Arg----Trp) at position 35 of the alpha I domainL Morlé, F Morlé, A F Roux, et al.Pageof 18