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H A Phillips

Showing results (41-50 of 47) with videos related to

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American Journal of Medical Genetics|June 5, 1995
Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic depositsH M Mitchison, A M O'Rawe, T J Lerner, et al.
Genomics|July 15, 1994
Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic associationH M Mitchison, P E Taschner, A M O'Rawe, et al.
American Journal of Human Genetics|February 1, 1993
Refined genetic localization for central core diseaseJ C Mulley, H M Kozman, H A Phillips, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Nature Genetics|August 11, 1998
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1BR H Wallace, D W Wang, R Singh, et al.
Neurology|April 14, 2004
LGI1 mutations in temporal lobe epilepsiesS F Berkovic, P Izzillo, J M McMahon, et al.
American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
American Journal of Medical Genetics|June 5, 1995
Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten disease with granular osmiophilic depositsH M Mitchison, A M O'Rawe, T J Lerner, et al.
Genomics|July 15, 1994
Genetic mapping of the Batten disease locus (CLN3) to the interval D16S288-D16S383 by analysis of haplotypes and allelic associationH M Mitchison, P E Taschner, A M O'Rawe, et al.
American Journal of Human Genetics|February 1, 1993
Refined genetic localization for central core diseaseJ C Mulley, H M Kozman, H A Phillips, et al.
American Journal of Human Genetics|December 6, 2000
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsyH A Phillips, I Favre, M Kirkpatrick, et al.
Nature Genetics|August 11, 1998
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1BR H Wallace, D W Wang, R Singh, et al.
Neurology|April 14, 2004
LGI1 mutations in temporal lobe epilepsiesS F Berkovic, P Izzillo, J M McMahon, et al.
American Journal of Human Genetics|October 3, 1998
Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24H A Phillips, I E Scheffer, K M Crossland, et al.
Pageof 5