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H M Mitchison

Showing results (21-30 of 34) with videos related to

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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.
Genomics|September 20, 1995
YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2I E Järvelä, H M Mitchison, A M O'Rawe, 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.
Cytogenetics and Cell Genetics|November 4, 2000
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)A K Maiti, L Bartoloni, H M Mitchison, 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.
Neuropediatrics|February 1, 1997
Structure of the CLN3 gene and predicted structure, location and function of CLN3 proteinH M Mitchison, P E Taschner, G Kremmidiotis, et al.
Journal of Medical Genetics|April 4, 2000
A locus for primary ciliary dyskinesia maps to chromosome 19qM Meeks, A Walne, S Spiden, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
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.
Genomics|September 20, 1995
YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2I E Järvelä, H M Mitchison, A M O'Rawe, 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.
Cytogenetics and Cell Genetics|November 4, 2000
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD)A K Maiti, L Bartoloni, H M Mitchison, 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.
Neuropediatrics|February 1, 1997
Structure of the CLN3 gene and predicted structure, location and function of CLN3 proteinH M Mitchison, P E Taschner, G Kremmidiotis, et al.
Journal of Medical Genetics|April 4, 2000
A locus for primary ciliary dyskinesia maps to chromosome 19qM Meeks, A Walne, S Spiden, et al.
Pageof 4