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Human Genetics|August 1, 1988
DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyriaJ S Lee, M Anvret, J Lindsten, 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 AnsvedJournal of Internal Medicine. Supplement|January 1, 1997
Understanding von Willebrand's disease from gene defects to the patientsZ Zhang, M Blombäck, M AnvretNucleic Acids Research|January 25, 1984
Evidence for integrated EBV genomes in Raji cellular DNAM Anvret, A Karlsson, G BjursellNeuromuscular Disorders : NMD|June 1, 1997
C4342T-mutation in the SCN4A gene on chromosome 17q in a Swedish family with paramyotonia congenita (Eulenburg)--correlations with clinical, neurophysiological and muscle biopsy dataK Borg, G Ahlberg, M AnvretHuman Genetics|February 1, 1994
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele originA Nordenskjöld, E Friedman, M AnvretNeurology|November 18, 1998
Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington diseaseT Ansved, A Lundin, M AnvretNeuropediatrics|December 1, 1994
Rett syndrome: the bcl-2 gene--a mediator of neurotrophic mechanisms?M Anvret, Z P Zhang, B HagbergJournal of Pediatric Surgery|July 1, 1996
No evidence of WT1 gene mutations in children with congenital diaphragmatic herniaA Nordenskjöld, M Tapper-Persson, M AnvretPageof 173