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A L Beaudet

Showing results (61-70 of 233) with videos related to

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Current Opinion in Genetics & Development|August 5, 1998
Imprinting in Angelman and Prader-Willi syndromesY Jiang, T F Tsai, J Bressler, et al.
Nucleic Acids Research|February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplificationH Northrup, C Rosenbloom, W E O'Brien, et al.
Clinical Genetics|October 1, 1982
Ornithine transcarbamylase deficiency: long-term survivalV V Michels, E Potts, M Walser, et al.
Pediatrics|May 1, 1993
Arginase deficiency presenting as cerebral palsyA E Scheuerle, R McVie, A L Beaudet, et al.
Genomics|March 20, 1995
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptorA Orr-Urtreger, M F Seldin, A Baldini, et al.
Lancet (London, England)|February 15, 2011
Identification of incestuous parental relationships by SNP-based DNA microarraysC P Schaaf, D A Scott, J Wiszniewska, et al.
Lancet (London, England)|July 9, 1988
Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphismG L Feldman, R Williamson, A L Beaudet, et al.
Molecular Biology & Medicine|April 1, 1989
Analysis of deletions at the human argininosuccinate synthetase locusM J Jackson, K Kobayashi, A L Beaudet, et al.
Human Mutation|January 1, 1995
Simultaneous analysis of mutant and normal alleles for multiple cystic fibrosis mutations by the ligase chain reactionP Fang, S Bouma, C Jou, et al.
Clinical Genetics|November 4, 2004
Autism in Angelman syndrome: implications for autism researchS U Peters, A L Beaudet, N Madduri, et al.
Pageof 24

Showing results (61-70 of 233) with videos related to

Sort By:
Pageof 24
Current Opinion in Genetics & Development|August 5, 1998
Imprinting in Angelman and Prader-Willi syndromesY Jiang, T F Tsai, J Bressler, et al.
Nucleic Acids Research|February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplificationH Northrup, C Rosenbloom, W E O'Brien, et al.
Clinical Genetics|October 1, 1982
Ornithine transcarbamylase deficiency: long-term survivalV V Michels, E Potts, M Walser, et al.
Pediatrics|May 1, 1993
Arginase deficiency presenting as cerebral palsyA E Scheuerle, R McVie, A L Beaudet, et al.
Genomics|March 20, 1995
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptorA Orr-Urtreger, M F Seldin, A Baldini, et al.
Lancet (London, England)|February 15, 2011
Identification of incestuous parental relationships by SNP-based DNA microarraysC P Schaaf, D A Scott, J Wiszniewska, et al.
Lancet (London, England)|July 9, 1988
Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphismG L Feldman, R Williamson, A L Beaudet, et al.
Molecular Biology & Medicine|April 1, 1989
Analysis of deletions at the human argininosuccinate synthetase locusM J Jackson, K Kobayashi, A L Beaudet, et al.
Human Mutation|January 1, 1995
Simultaneous analysis of mutant and normal alleles for multiple cystic fibrosis mutations by the ligase chain reactionP Fang, S Bouma, C Jou, et al.
Clinical Genetics|November 4, 2004
Autism in Angelman syndrome: implications for autism researchS U Peters, A L Beaudet, N Madduri, et al.
Pageof 24