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M Anvret

Showing results (31-40 of 138) with videos related to

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Lakartidningen|July 24, 1991
[Mutation diagnosis is a possibility for the half of the families with acute intermittent porphyria]M Anvret, J S Lee, G Lundin
Lakartidningen|October 21, 1992
[Familial adenomatous polyposis. The gene of the disease was recently isolated--the pathogenesis of colonic cancer can be explained]R Hultcrantz, T Alm, M Anvret, et al.
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.
Lakartidningen|September 23, 1992
[Increasing number of hemoglobinopathies. Rapid diagnosis with DNA technique]T H Bui, M Anvret, K Bröndum-Nielsen
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.
Lakartidningen|October 1, 1986
[Retinitis pigmentosa--more families are needed to localize the genes]J Gyftodimou, M Anvret, P Goonewardena, 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.
Pageof 14

Showing results (31-40 of 138) with videos related to

Sort By:
Pageof 14
Lakartidningen|July 24, 1991
[Mutation diagnosis is a possibility for the half of the families with acute intermittent porphyria]M Anvret, J S Lee, G Lundin
Lakartidningen|October 21, 1992
[Familial adenomatous polyposis. The gene of the disease was recently isolated--the pathogenesis of colonic cancer can be explained]R Hultcrantz, T Alm, M Anvret, et al.
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.
Lakartidningen|September 23, 1992
[Increasing number of hemoglobinopathies. Rapid diagnosis with DNA technique]T H Bui, M Anvret, K Bröndum-Nielsen
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.
Lakartidningen|October 1, 1986
[Retinitis pigmentosa--more families are needed to localize the genes]J Gyftodimou, M Anvret, P Goonewardena, 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.
Pageof 14