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J Gusella

Showing results (21-30 of 32) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1979
Precise localization of human beta-globin gene complex on chromosome 11J Gusella, A Varsanyi-Breiner, F T Kao, et al.
Journal of Medical Genetics|November 1, 1994
Trinucleotide repeat length and progression of illness in Huntington's diseaseK Kieburtz, M MacDonald, C Shih, et al.
Genomics|March 1, 1993
A set of STS assays targeting the chromosome 22 physical framework markersM MacCollin, D Romano, M Budarf, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
Genomics|January 15, 1994
CEPH consortium Map of chromosome 9J Attwood, M Chiano, A Collins, et al.
Genomics|January 1, 1995
The CEPH consortium linkage map of human chromosome 16H M Kozman, T P Keith, H Donis-Keller, et al.
Annals of Neurology|September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genesT Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology|November 1, 1990
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Archives of Neurology|November 1, 1992
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1979
Precise localization of human beta-globin gene complex on chromosome 11J Gusella, A Varsanyi-Breiner, F T Kao, et al.
Journal of Medical Genetics|November 1, 1994
Trinucleotide repeat length and progression of illness in Huntington's diseaseK Kieburtz, M MacDonald, C Shih, et al.
Genomics|March 1, 1993
A set of STS assays targeting the chromosome 22 physical framework markersM MacCollin, D Romano, M Budarf, et al.
Molecular and Cellular Probes|December 1, 1992
Assay by polymerase chain reaction (PCR) of multi-allele polymorphisms in the Huntington's disease region of chromosome 4B A Allitto, A I McClatchey, G Barnes, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
Genomics|January 15, 1994
CEPH consortium Map of chromosome 9J Attwood, M Chiano, A Collins, et al.
Genomics|January 1, 1995
The CEPH consortium linkage map of human chromosome 16H M Kozman, T P Keith, H Donis-Keller, et al.
Annals of Neurology|September 1, 1994
Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genesT Gasser, Z K Wszolek, J Trofatter, et al.
Annals of Neurology|November 1, 1990
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Archives of Neurology|November 1, 1992
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Pageof 4