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F Lennon

Showing results (51-60 of 71) with videos related to

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Investigative Ophthalmology & Visual Science|May 1, 1997
Exclusion of TIMP3 as a candidate locus in age-related macular degenerationM A De La Paz, M A Pericak-Vance, F Lennon, et al.
Computers and Biomedical Research, an International Journal|June 1, 1995
Computer-assisted mapping of infarcted and viable regions of gross cardiac sections following experimental myocardial infarctionC J Damm, J T Bigger, P C Ursell, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
American Journal of Human Genetics|April 1, 1996
Linkage of a gene for macular corneal dystrophy to chromosome 16J M Vance, F Jonasson, F Lennon, et al.
The British Journal of Ophthalmology|May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibshipN P Liu, J Baldwin, F Lennon, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
American Journal of Human Genetics|July 1, 1996
Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2BJ M Vance, M C Speer, J M Stajich, et al.
American Journal of Human Genetics|August 27, 1998
Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I geneN P Liu, J Baldwin, F Jonasson, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Investigative Ophthalmology & Visual Science|May 1, 1997
Exclusion of TIMP3 as a candidate locus in age-related macular degenerationM A De La Paz, M A Pericak-Vance, F Lennon, et al.
Computers and Biomedical Research, an International Journal|June 1, 1995
Computer-assisted mapping of infarcted and viable regions of gross cardiac sections following experimental myocardial infarctionC J Damm, J T Bigger, P C Ursell, et al.
Human Heredity|November 14, 1998
Evidence for genetic heterogeneity supports clinical differences in congenital myasthenic syndromesM M Menold, M Sadeh, F Lennon, et al.
American Journal of Human Genetics|April 1, 1996
Linkage of a gene for macular corneal dystrophy to chromosome 16J M Vance, F Jonasson, F Lennon, et al.
The British Journal of Ophthalmology|May 29, 1998
Coexistence of macular corneal dystrophy types I and II in a single sibshipN P Liu, J Baldwin, F Lennon, et al.
Human Molecular Genetics|October 1, 1993
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8qK Ben Othmane, F Hentati, F Lennon, et al.
Human Molecular Genetics|October 1, 1994
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersA Hentati, M A Pericak-Vance, F Lennon, et al.
American Journal of Human Genetics|July 1, 1996
Misclassification and linkage of hereditary sensory and autonomic neuropathy type 1 as Charcot-Marie-Tooth disease, type 2BJ M Vance, M C Speer, J M Stajich, et al.
American Journal of Human Genetics|August 27, 1998
Haplotype analysis in Icelandic families defines a minimal interval for the macular corneal dystrophy type I geneN P Liu, J Baldwin, F Jonasson, et al.
Neurology|March 1, 1992
Linkage studies in Charcot-Marie-Tooth disease type 2: evidence that CMT types 1 and 2 are distinct genetic entitiesL J Loprest, M A Pericak-Vance, J Stajich, et al.
Pageof 8