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Proceedings of the National Academy of Sciences of the United States of America|December 1, 1991
Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyriaJ S Lee, M AnvretHuman Genetics|February 1, 1990
Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reactionJ S Lee, J Lindsten, M AnvretHuman Genetics|July 1, 1997
Genetic investigation of the porphobilinogen deaminase gene in Swedish acute intermittent porphyria familiesG Lundin, J S Lee, S Thunell, et al.Human Genetics|August 1, 1991
Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyriaJ S Lee, G Lundin, L Lannfelt, et al.American Journal of Medical Genetics. Supplement|January 1, 1986
Chromosome findings in the Rett syndrome and a test of a two-step mutation theoryJ Wahlström, M AnvretBiochemical and Biophysical Research Communications|February 13, 1997
Characterization and regulation of the nonerythroid porphobilinogen deaminase promoterG Lundin, M AnvretPageof 173