Showing results (51-60 of 579) with videos related to
Sort By:
Pageof 58
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Identification of the binding domain for NADP+ of human glucose-6-phosphate dehydrogenase by sequence analysis of mutantsA Hirono, W Kuhl, T Gelbart, et al.Blood Cells, Molecules & Diseases|January 11, 2002
A study of genes that may modulate the expression of hereditary hemochromatosis: transferrin receptor-1, ferroportin, ceruloplasmin, ferritin light and heavy chains, iron regulatory proteins (IRP)-1 and -2, and hepcidinP L Lee, T Gelbart, C West, et al.Hemoglobin|January 1, 1995
A novel intrachromosomal rearrangement in the beta-globin gene found in an African-American familyS Rahbar, G Nozari, G Forrest, et al.Genomics|July 15, 1997
Three genes encoding zinc finger proteins on human chromosome 6p21.3: members of a new subclass of the Kruppel gene family containing the conserved SCAN box domainP L Lee, T Gelbart, C West, et al.Blood|July 10, 1998
Six previously undescribed pyruvate kinase mutations causing enzyme deficiencyA Demina, K I Varughese, J Barbot, et al.Medicine|November 1, 1992
Gaucher disease. Clinical, laboratory, radiologic, and genetic features of 53 patientsA Zimran, A Kay, T Gelbart, et al.Blood|December 9, 2000
Molecular characterization of a case of atransferrinemiaE Beutler, T Gelbart, P Lee, et al.Human Genetics|June 1, 1997
Molecular analysis of Gaucher disease: distribution of eight mutations and the complete gene deletion in 27 patients from GermanyP le Coutre, A Demina, E Beutler, et al.Blood Cells, Molecules & Diseases|December 9, 2000
A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypesM Iancovici-Kidon, D Sthoeger, A Abrahamov, et al.American Journal of Human Genetics|January 1, 1993
Gaucher disease: gene frequencies in the Ashkenazi Jewish populationE Beutler, N J Nguyen, M W Henneberger, et al.Pageof 58