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C C Morton

Showing results (161-170 of 185) with videos related to

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Genes, Chromosomes & Cancer|May 29, 2000
A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosisC J Vaughan, S Weremowicz, M M Goldstein, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14G M Caldwell, R L Eddy, C D Day, et al.
Genomics|October 14, 2000
SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseasesC N Adra, J L Donato, R Badovinac, et al.
Molecular Cell|January 10, 2002
Impaired nonhomologous end-joining provokes soft tissue sarcomas harboring chromosomal translocations, amplifications, and deletionsN E Sharpless, D O Ferguson, R C O'Hagan, et al.
Journal of Medical Genetics|November 25, 2003
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutationA Iannaccone, D K Breuer, X F Wang, et al.
Genomics|October 27, 1998
Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3C N Adra, A R Iyengar, F A Syed, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 17, 2005
Characterization of familial Waldenstrom's macroglobulinemiaS P Treon, Z R Hunter, A Aggarwal, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
Pageof 19

Showing results (161-170 of 185) with videos related to

Sort By:
Pageof 19
Genes, Chromosomes & Cancer|May 29, 2000
A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosisC J Vaughan, S Weremowicz, M M Goldstein, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14G M Caldwell, R L Eddy, C D Day, et al.
Genomics|October 14, 2000
SMARCAD1, a novel human helicase family-defining member associated with genetic instability: cloning, expression, and mapping to 4q22-q23, a band rich in breakpoints and deletion mutants involved in several human diseasesC N Adra, J L Donato, R Badovinac, et al.
Molecular Cell|January 10, 2002
Impaired nonhomologous end-joining provokes soft tissue sarcomas harboring chromosomal translocations, amplifications, and deletionsN E Sharpless, D O Ferguson, R C O'Hagan, et al.
Journal of Medical Genetics|November 25, 2003
Clinical and immunohistochemical evidence for an X linked retinitis pigmentosa syndrome with recurrent infections and hearing loss in association with an RPGR mutationA Iannaccone, D K Breuer, X F Wang, et al.
Genomics|October 27, 1998
Human ARHGDIG, a GDP-dissociation inhibitor for Rho proteins: genomic structure, sequence, expression analysis, and mapping to chromosome 16p13.3C N Adra, A R Iyengar, F A Syed, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|December 17, 2005
Characterization of familial Waldenstrom's macroglobulinemiaS P Treon, Z R Hunter, A Aggarwal, et al.
Human Molecular Genetics|July 13, 1999
High prevalence of symptoms of Menière's disease in three families with a mutation in the COCH geneE Fransen, M Verstreken, W I Verhagen, et al.
Science (New York, N.Y.)|April 16, 1998
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humansO Vahava, R Morell, E D Lynch, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
Pageof 19