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M Anvret

Showing results (111-120 of 138) with videos related to

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The New England Journal of Medicine|February 18, 1993
Direct diagnosis of myotonic dystrophy with a disease-specific DNA markerP Shelbourne, J Davies, J Buxton, et al.
Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.
Antisense & Nucleic Acid Drug Development|January 26, 1999
Failure to achieve gene conversion with chimeric circular oligonucleotides: potentially misleading PCR artifacts observedZ Zhang, M Eriksson, G Falk, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1997
Treatment of adrenoleukodystrophy with bone marrow transplantationG Malm, O Ringdén, M Anvret, et al.
Nature Genetics|February 1, 1994
Meiotic drive at the myotonic dystrophy locus?N Carey, K Johnson, P Nokelainen, et al.
Journal of Medical Genetics|May 23, 1998
Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of XqF Xiang, Z Zhang, A Clarke, et al.
American Journal of Human Genetics|June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusK Johnson, P Shelbourne, J Davies, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Genetics|January 1, 1993
X chromosome linkage studies in familial Rett syndromeA R Curtis, S Headland, S Lindsay, et al.
Pageof 14

Showing results (111-120 of 138) with videos related to

Sort By:
Pageof 14
The New England Journal of Medicine|February 18, 1993
Direct diagnosis of myotonic dystrophy with a disease-specific DNA markerP Shelbourne, J Davies, J Buxton, et al.
Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.
Antisense & Nucleic Acid Drug Development|January 26, 1999
Failure to achieve gene conversion with chimeric circular oligonucleotides: potentially misleading PCR artifacts observedZ Zhang, M Eriksson, G Falk, et al.
Clinical Genetics|June 1, 1993
DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington diseaseS Andrew, J Theilmann, E Almqvist, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 1, 1997
Treatment of adrenoleukodystrophy with bone marrow transplantationG Malm, O Ringdén, M Anvret, et al.
Nature Genetics|February 1, 1994
Meiotic drive at the myotonic dystrophy locus?N Carey, K Johnson, P Nokelainen, et al.
Journal of Medical Genetics|May 23, 1998
Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of XqF Xiang, Z Zhang, A Clarke, et al.
American Journal of Human Genetics|June 1, 1990
A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locusK Johnson, P Shelbourne, J Davies, et al.
American Journal of Human Genetics|May 1, 1994
Huntington disease without CAG expansion: phenocopies or errors in assignment?S E Andrew, Y P Goldberg, B Kremer, et al.
Human Genetics|January 1, 1993
X chromosome linkage studies in familial Rett syndromeA R Curtis, S Headland, S Lindsay, et al.
Pageof 14