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Showing results (41-50 of 54) with videos related to

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Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Neurology|February 17, 2010
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCLW Xin, T E Mullen, R Kiely, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8W A Mitchell, R B Wheeler, J D Sharp, et al.
Neurology|February 25, 2005
A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onsetN Pineda-Trujillo, W Cornejo, J Carrizosa, et al.
American Journal of Human Genetics|March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypesH M Mitchison, A M O'Rawe, P E Taschner, et al.
Neurology|February 5, 1999
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosisL Lauronen, P B Munroe, I Järvelä, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Molecular Genetics and Metabolism|April 7, 1999
The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in ScotlandJ B Stephenson, N D Greene, K Y Leung, et al.
American Journal of Human Genetics|August 1, 1997
Spectrum of mutations in the Batten disease gene, CLN3P B Munroe, H M Mitchison, A M O'Rawe, et al.
Pageof 6

Showing results (41-50 of 54) with videos related to

Sort By:
Pageof 6
Nature|June 3, 1993
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2AL M Mulligan, J B Kwok, C S Healey, et al.
Neurology|February 17, 2010
CLN5 mutations are frequent in juvenile and late-onset non-Finnish patients with NCLW Xin, T E Mullen, R Kiely, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
Turkish variant late infantile neuronal ceroid lipofuscinosis (CLN7) may be allelic to CLN8W A Mitchell, R B Wheeler, J D Sharp, et al.
Neurology|February 25, 2005
A CLN5 mutation causing an atypical neuronal ceroid lipofuscinosis of juvenile onsetN Pineda-Trujillo, W Cornejo, J Carrizosa, et al.
American Journal of Human Genetics|March 1, 1995
Batten disease gene, CLN3: linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypesH M Mitchison, A M O'Rawe, P E Taschner, et al.
Neurology|February 5, 1999
Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosisL Lauronen, P B Munroe, I Järvelä, et al.
Molecular Genetics and Metabolism|April 7, 1999
A murine model for juvenile NCL: gene targeting of mouse Cln3N D Greene, D L Bernard, P E Taschner, et al.
Neuropediatrics|February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic depositsA O'Rawe, H M Mitchison, R Williams, et al.
Molecular Genetics and Metabolism|April 7, 1999
The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in ScotlandJ B Stephenson, N D Greene, K Y Leung, et al.
American Journal of Human Genetics|August 1, 1997
Spectrum of mutations in the Batten disease gene, CLN3P B Munroe, H M Mitchison, A M O'Rawe, et al.
Pageof 6