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M Anvret

Showing results (61-70 of 138) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.
Annals of Neurology|September 11, 1999
Genetic linkage of Welander distal myopathy to chromosome 2p13G Ahlberg, D von Tell, K Borg, et al.
Genomics|May 1, 1994
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish originZ P Zhang, M Blombäck, N Egberg, et al.
Brain & Development|January 1, 1990
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureJ Wahlström, I Witt-Engerström, L Mellquist, et al.
Human Molecular Genetics|December 1, 1992
A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patientsZ P Zhang, G Falk, M Blombäck, et al.
Lakartidningen|January 27, 1993
[The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis]E S Blennow, T H Bui, S Söderhäll, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Alcohol dehydrogenase alleles in Parkinson's diseaseS Buervenich, O Sydow, A Carmine, et al.
Neuromuscular Disorders : NMD|July 17, 1999
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21F Xiang, P Nicolao, F Chapon, et al.
Clinical Genetics|January 1, 1993
Hemophilia B in a 46,XX female probably caused by non-random X inactivationC Wadelius, M Lindstedt, M Pigg, et al.
Human Molecular Genetics|September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyM Anvret, G Ahlberg, U Grandell, et al.
Pageof 14

Showing results (61-70 of 138) with videos related to

Sort By:
Pageof 14
Acta Paediatrica (Oslo, Norway : 1992)|December 1, 1996
Achondroplasia in Sweden caused by the G1138A mutation in FGFR3A Alderborn, M Anvret, K H Gustavson, et al.
Annals of Neurology|September 11, 1999
Genetic linkage of Welander distal myopathy to chromosome 2p13G Ahlberg, D von Tell, K Borg, et al.
Genomics|May 1, 1994
Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish originZ P Zhang, M Blombäck, N Egberg, et al.
Brain & Development|January 1, 1990
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureJ Wahlström, I Witt-Engerström, L Mellquist, et al.
Human Molecular Genetics|December 1, 1992
A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patientsZ P Zhang, G Falk, M Blombäck, et al.
Lakartidningen|January 27, 1993
[The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis]E S Blennow, T H Bui, S Söderhäll, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Alcohol dehydrogenase alleles in Parkinson's diseaseS Buervenich, O Sydow, A Carmine, et al.
Neuromuscular Disorders : NMD|July 17, 1999
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21F Xiang, P Nicolao, F Chapon, et al.
Clinical Genetics|January 1, 1993
Hemophilia B in a 46,XX female probably caused by non-random X inactivationC Wadelius, M Lindstedt, M Pigg, et al.
Human Molecular Genetics|September 1, 1993
Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophyM Anvret, G Ahlberg, U Grandell, et al.
Pageof 14