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P F Chance

Showing results (61-70 of 78) with videos related to

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Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Human Mutation|March 3, 1998
Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeatM Yamamoto, M P Keller, T Yasuda, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Genomics|April 7, 1999
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease lociL M Kalikin, R A George, M P Keller, et al.
Neurology|October 1, 1995
New connexin32 mutations associated with X-linked Charcot-Marie-Tooth diseaseL J Bone, N Dahl, M W Lensch, et al.
Immunogenetics|October 31, 2001
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndromeC L Bennett, M E Brunkow, F Ramsdell, et al.
Science (New York, N.Y.)|December 24, 1993
Connexin mutations in X-linked Charcot-Marie-Tooth diseaseJ Bergoffen, S S Scherer, S Wang, et al.
Nature Genetics|January 4, 2001
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3C L Bennett, J Christie, F Ramsdell, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
Nature Genetics|September 1, 1993
Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 geneK Hayasaka, M Himoro, W Sato, et al.
Human Mutation|March 3, 1998
Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeatM Yamamoto, M P Keller, T Yasuda, et al.
Neurogenetics|November 21, 2000
A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4) localizes to a 500-kb interval on chromosome 9q34I P Blair, C L Bennett, A Abel, et al.
Genomics|April 7, 1999
An integrated physical and gene map of human distal chromosome 17q24-proximal 17q25 encompassing multiple disease lociL M Kalikin, R A George, M P Keller, et al.
Neurology|October 1, 1995
New connexin32 mutations associated with X-linked Charcot-Marie-Tooth diseaseL J Bone, N Dahl, M W Lensch, et al.
Immunogenetics|October 31, 2001
A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndromeC L Bennett, M E Brunkow, F Ramsdell, et al.
Science (New York, N.Y.)|December 24, 1993
Connexin mutations in X-linked Charcot-Marie-Tooth diseaseJ Bergoffen, S S Scherer, S Wang, et al.
Nature Genetics|January 4, 2001
The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3C L Bennett, J Christie, F Ramsdell, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Pageof 8