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M Anvret

Showing results (121-130 of 138) with videos related to

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Lakartidningen|October 17, 1990
[Diagnosis of cystic fibrosis by means of genetic technology--guidelines from an expert meeting]J Wahlström, G Annerén, M Anvret, et al.
Human Molecular Genetics|October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parentH Telenius, H P Kremer, J Theilmann, et al.
Human Molecular Genetics|February 1, 1995
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington diseaseE Almqvist, N Spence, K Nichol, et al.
Nature|February 6, 1992
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyJ Buxton, P Shelbourne, J Davies, et al.
Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.
American Journal of Human Genetics|March 1, 1994
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.
American Journal of Human Genetics|February 1, 1992
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisK A Ellison, C P Fill, J Terwilliger, et al.
Lakartidningen|August 27, 1997
[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]E Iwarsson, E S Blennow, M Anvret, et al.
Genes and Immunity|January 28, 2005
Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosisZ Zhang, K Duvefelt, F Svensson, et al.
Journal of Medical Genetics|July 4, 2001
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.
Pageof 14

Showing results (121-130 of 138) with videos related to

Sort By:
Pageof 14
Lakartidningen|October 17, 1990
[Diagnosis of cystic fibrosis by means of genetic technology--guidelines from an expert meeting]J Wahlström, G Annerén, M Anvret, et al.
Human Molecular Genetics|October 1, 1993
Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parentH Telenius, H P Kremer, J Theilmann, et al.
Human Molecular Genetics|February 1, 1995
Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington diseaseE Almqvist, N Spence, K Nichol, et al.
Nature|February 6, 1992
Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophyJ Buxton, P Shelbourne, J Davies, et al.
Human Genetics|December 1, 1988
Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19qK Johnson, E Nimmo, P Jones, et al.
American Journal of Human Genetics|March 1, 1994
Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophyT Ashizawa, M Anvret, M Baiget, et al.
American Journal of Human Genetics|February 1, 1992
Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisK A Ellison, C P Fill, J Terwilliger, et al.
Lakartidningen|August 27, 1997
[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis]E Iwarsson, E S Blennow, M Anvret, et al.
Genes and Immunity|January 28, 2005
Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosisZ Zhang, K Duvefelt, F Svensson, et al.
Journal of Medical Genetics|July 4, 2001
Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the diseaseL Villard, N Lévy, F Xiang, et al.
Pageof 14