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Neuromuscular Disorders : NMD|June 3, 1998
Welander distal myopathy--an overviewK Borg, G Ahlberg, M Anvret, et al.American Journal of Hematology|June 1, 1992
On laboratory problems in diagnosing mild von Willebrand's diseaseM Blombäck, P Eneroth, O Andersson, et al.Neuropediatrics|September 26, 2001
Closely related Swedish Rett Syndrome females - none with MECP2 mutation revealedF Xiang, Y Stenbom, M Anvret, et al.Neuromuscular Disorders : NMD|June 1, 1997
Welander distal myopathy is not linked to other defined distal myopathy gene lociG Ahlberg, K Borg, L Edström, et al.Neuromuscular Disorders : NMD|June 3, 1998
Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodiesG Ahlberg, K Borg, L Edström, et al.Human Genetics|January 1, 1994
Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific allelesG Lundin, A Wedell, S Thunell, et al.Biochemical and Biophysical Research Communications|March 10, 2001
A mammalian radial spokehead-like gene, RSHL1, at the myotonic dystrophy-1 locusM Eriksson, T Ansved, M Anvret, et al.American Journal of Medical Genetics|September 1, 1990
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generationsM Anvret, J Wahlström, P Skogsberg, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|June 2, 1998
A new approach to gene therapyZ Zhang, M Eriksson, M Blombäck, et al.Human Genetics|October 1, 1995
Effects of the mutant von Willebrand factor gene in von Willebrand diseaseZ Zhang, M Lindstedt, M Blombäck, et al.Pageof 173