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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 AnvretProceedings 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 AnvretAmerican Journal of Human Genetics|October 11, 2001
Huntington disease phenocopy is a familial prion diseaseR C Moore, F Xiang, J Monaghan, et al.American Journal of Human Genetics|October 30, 1998
A Huntington disease-like neurodegenerative disorder maps to chromosome 20pF Xiang, E W Almqvist, M Huq, et al.Human Genetics|July 1, 1995
Absence of mutations in the WT1 gene in patients with XY gonadal dysgenesisA Nordenskjöld, G Fricke, M AnvretEuropean Journal of Neurology|April 22, 1999
CTG-repeat length in distal and proximal leg muscles of symptomatic and non-symptomatic patients with myotonic dystrophy: relation to muscle strength and degree of histopathological abnormalitiesB Hedberg, M Anvret, T AnsvedPageof 18