J J Wasmuth - JoVE Visualize

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1992

Chromosomal localization of human glutamate receptor genesJ O McNamara, J H Eubanks, J D McPherson, et al.

American Journal of Medical Genetics|November 1, 1992

Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndromeM R Altherr, J F Gusella, J J Wasmuth, et al.

Nature|April 21, 1988

A highly polymorphic locus very tightly linked to the Huntington's disease geneJ J Wasmuth, J Hewitt, B Smith, et al.

Human Molecular Genetics|February 1, 1994

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndromeJ Overhauser, X Huang, M Gersh, et al.

Human Molecular Genetics|October 1, 1996

Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the geneA J Gladwin, J Dixon, S K Loftus, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990

Expression and chromosomal localization of a lymphocyte K+ channel geneS Grissmer, B Dethlefs, J J Wasmuth, et al.

Genomics|December 1, 1991

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4L M Thompson, S Plummer, M Schalling, et al.

Genomics|November 1, 1993

Molecular cloning of the human proto-oncogene Wnt-5A and mapping of the gene (WNT5A) to chromosome 3p14-p21C C Clark, I Cohen, I Eichstetter, et al.

Human Molecular Genetics|October 1, 1996

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD regionS T Winokur, U Bengtsson, J C Vargas, et al.

Molecular and Cellular Biology|September 1, 1996

The Ras GTPase-activating-protein-related human protein IQGAP2 harbors a potential actin binding domain and interacts with calmodulin and Rho family GTPasesS Brill, S Li, C W Lyman, et al.

Pageof 14

Showing results (61-70 of 133) with videos related to

Sort By:

Pageof 14

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 1, 1992

Chromosomal localization of human glutamate receptor genesJ O McNamara, J H Eubanks, J D McPherson, et al.

American Journal of Medical Genetics|November 1, 1992

Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndromeM R Altherr, J F Gusella, J J Wasmuth, et al.

Nature|April 21, 1988

A highly polymorphic locus very tightly linked to the Huntington's disease geneJ J Wasmuth, J Hewitt, B Smith, et al.

Human Molecular Genetics|February 1, 1994

Molecular and phenotypic mapping of the short arm of chromosome 5: sublocalization of the critical region for the cri-du-chat syndromeJ Overhauser, X Huang, M Gersh, et al.

Human Molecular Genetics|October 1, 1996

Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the geneA J Gladwin, J Dixon, S K Loftus, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 1, 1990

Expression and chromosomal localization of a lymphocyte K+ channel geneS Grissmer, B Dethlefs, J J Wasmuth, et al.

Genomics|December 1, 1991

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4L M Thompson, S Plummer, M Schalling, et al.

Genomics|November 1, 1993

Molecular cloning of the human proto-oncogene Wnt-5A and mapping of the gene (WNT5A) to chromosome 3p14-p21C C Clark, I Cohen, I Eichstetter, et al.

Human Molecular Genetics|October 1, 1996

The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD regionS T Winokur, U Bengtsson, J C Vargas, et al.

Molecular and Cellular Biology|September 1, 1996

The Ras GTPase-activating-protein-related human protein IQGAP2 harbors a potential actin binding domain and interacts with calmodulin and Rho family GTPasesS Brill, S Li, C W Lyman, et al.

Pageof 14