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Acta Haematologica|January 1, 1978
Congenital methemoglobin-reductase (cytochrome b5 reductase) deficiency associated with mental retardation in a Spanish girlJ L Vives-Corrons, A Pujades, E Vela, et al.Biochemical and Biophysical Research Communications|April 15, 1993
Expression of the dystrophin gene in cultured fibroblastsJ P Hugnot, H Gilgenkrantz, P Chafey, et al.Human Genetics|January 19, 1978
Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variantsM Benabadji, F Merad, M Benmoussa, et al.American Journal of Human Genetics|March 1, 1990
The red-green visual pigment gene region in adrenoleukodystrophyP Aubourg, R Feil, S Guidoux, et al.Annales De Medecine Interne|November 1, 1977
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]F Nouailhat, J C Kaplan, Y Giudicelli, et al.American Journal of Human Genetics|February 1, 1988
A linkage and physical map of chromosome 22, and some applications to gene mappingC Julier, G M Lathrop, A Reghis, et al.Human Genetics|November 1, 1986
De novo mutation in hemophilia A established by DNA haplotype analysis and precluding prenatal diagnosisM Delpech, N Deburgrave, M Baudis, et al.Nucleic Acids Research|June 11, 1987
Clustered somatic mutations in and around first exon of non-rearranged c-myc in Burkitt lymphoma with t(8;22) translocationM F Szajnert, S Saule, G W Bornkamm, et al.Acta Haematologica|January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotesA Mast, R Milo, C Junien, et al.Human Genetics|March 1, 1988
Nebulin seen in DMD males including one patient with a large DNA deletion encompassing the DMD geneJ J Pernelle, P Chafey, J Chelly, et al.Pageof 19