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Birth Defects Original Article Series|January 1, 1982
The pattern of thalassemia in NaplesG Pepe, L Lupi, A Mastrobuono, et al.Clinical and Experimental Immunology|July 1, 1988
The establishment of cell lines from chronic B cell leukaemias: evidence of leukaemic origin by karyotypic abnormalities and Ig gene rearrangementJ V Melo, L Foroni, V Brito-Babapulle, et al.Blood|December 15, 1992
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangementsI Dokal, J Bungey, P Williamson, et al.The New England Journal of Medicine|November 9, 1995
Natural history of paroxysmal nocturnal hemoglobinuriaP Hillmen, S M Lewis, M Bessler, et al.British Journal of Haematology|September 1, 1995
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD geneA Rovira, T Vulliamy, M A Pujades, et al.Human Genetics|April 1, 1993
G6PD Mediterranean accounts for the high prevalence of G6PD deficiency in Kurdish JewsA Oppenheim, C L Jury, D Rund, et al.Gene|September 16, 1996
High-level regulated expression of the human G6PD gene in transgenic miceC M Corcoran, P Fraser, G Martini, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Evaluation of iron overload in thalassemia]A Piga, S Davico, M Magliano, et al.Blood|October 6, 1997
Retrovirally transduced human dendritic cells express a normal phenotype and potent T-cell stimulatory capacityP Szabolcs, H F Gallardo, D H Ciocon, et al.Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase IIM N Fukuda, K A Masri, A Dell, et al.Pageof 22