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L Beaudet

Showing results (351-360 of 456) with videos related to

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Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 8, 2007
Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapyNicola Brunetti-Pierri, Gary E Stapleton, Donna J Palmer, et al.
Genome Research|April 1, 1997
The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical regionJ S Sutcliffe, Y H Jiang, R J Galijaard, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Evaluation of gene therapy for citrullinaemia using murine and bovine modelsG Patejunas, B Lee, J A Dennis, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 10, 2003
Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndromeEdwin J Weeber, Yong-Hui Jiang, Ype Elgersma, et al.
Journal of Medical Genetics|September 27, 2005
Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlationsT Sahoo, S U Peters, N S Madduri, et al.
The New England Journal of Medicine|February 1, 1990
Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Angelman syndrome 2005: updated consensus for diagnostic criteriaCharles A Williams, Arthur L Beaudet, Jill Clayton-Smith, et al.
The Journal of Pediatrics|August 5, 2006
Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesityJennifer Miller, John Kranzler, Yijun Liu, et al.
Pageof 46

Showing results (351-360 of 456) with videos related to

Sort By:
Pageof 46
Nature Genetics|July 1, 1993
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1H T Orr, M Y Chung, S Banfi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 8, 2007
Pseudo-hydrodynamic delivery of helper-dependent adenoviral vectors into non-human primates for liver-directed gene therapyNicola Brunetti-Pierri, Gary E Stapleton, Donna J Palmer, et al.
Genome Research|April 1, 1997
The E6-Ap ubiquitin-protein ligase (UBE3A) gene is localized within a narrowed Angelman syndrome critical regionJ S Sutcliffe, Y H Jiang, R J Galijaard, et al.
American Journal of Medical Genetics|November 1, 1988
Prenatal detection of 46,XY,rec(5),dup q, inv(5)(p13q33) using DNA analysis, flow cytometry, and in situ hybridization to supplement classical cytogenetic analysisA O Martin, H Northrup, D H Ledbetter, et al.
Journal of Inherited Metabolic Disease|August 1, 1998
Evaluation of gene therapy for citrullinaemia using murine and bovine modelsG Patejunas, B Lee, J A Dennis, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 10, 2003
Derangements of hippocampal calcium/calmodulin-dependent protein kinase II in a mouse model for Angelman mental retardation syndromeEdwin J Weeber, Yong-Hui Jiang, Ype Elgersma, et al.
Journal of Medical Genetics|September 27, 2005
Microarray based comparative genomic hybridization testing in deletion bearing patients with Angelman syndrome: genotype-phenotype correlationsT Sahoo, S U Peters, N S Madduri, et al.
The New England Journal of Medicine|February 1, 1990
Mutation analysis for heterozygote detection and the prenatal diagnosis of cystic fibrosisW K Lemna, G L Feldman, B Kerem, et al.
American Journal of Medical Genetics. Part A|February 14, 2006
Angelman syndrome 2005: updated consensus for diagnostic criteriaCharles A Williams, Arthur L Beaudet, Jill Clayton-Smith, et al.
The Journal of Pediatrics|August 5, 2006
Neurocognitive findings in Prader-Willi syndrome and early-onset morbid obesityJennifer Miller, John Kranzler, Yijun Liu, et al.
Pageof 46