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Showing results (101-110 of 110) with videos related to

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Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.
Lancet (London, England)|November 14, 1987
Inherited deletion at Duchenne dystrophy locus in normal maleJ Koh, R J Bartlett, M A Pericak-Vance, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.
Human Molecular Genetics|December 26, 2001
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1R Weksberg, J Nishikawa, O Caluseriu, et al.
Clinical Genetics|August 8, 2008
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in NewfoundlandS J Moore, D J Buckley, A MacMillan, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
JAMA|May 20, 1992
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter studyJ S Chamberlain, J R Chamberlain, R G Fenwick, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 11

Showing results (101-110 of 110) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 110 results.
Science (New York, N.Y.)|November 4, 1988
Frame-shift deletions in patients with Duchenne and Becker muscular dystrophyS B Malhotra, K A Hart, H J Klamut, et al.
Lancet (London, England)|November 14, 1987
Inherited deletion at Duchenne dystrophy locus in normal maleJ Koh, R J Bartlett, M A Pericak-Vance, et al.
American Journal of Human Genetics|August 1, 1992
Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qterC Wijmenga, L A Sandkuijl, P Moerer, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndromeD A Pillers, W K Seltzer, B R Powell, et al.
Human Molecular Genetics|December 26, 2001
Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1R Weksberg, J Nishikawa, O Caluseriu, et al.
Clinical Genetics|August 8, 2008
The clinical and genetic epidemiology of neuronal ceroid lipofuscinosis in NewfoundlandS J Moore, D J Buckley, A MacMillan, et al.
Human Genetics|September 10, 1999
Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutationsD A Pillers, K M Fitzgerald, N M Duncan, et al.
Molecular Genetics and Metabolism|March 9, 1999
Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutantsD A Pillers, R G Weleber, D G Green, et al.
JAMA|May 20, 1992
Diagnosis of Duchenne and Becker muscular dystrophies by polymerase chain reaction. A multicenter studyJ S Chamberlain, J R Chamberlain, R G Fenwick, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 11