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R J Smith

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Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|December 24, 1997
Imported yellow fever in a United States citizenJ M McFarland, L M Baddour, J E Nelson, et al.
Nature|December 6, 2013
Highly polarized light from stable ordered magnetic fields in GRB 120308AC G Mundell, D Kopač, D M Arnold, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Clinical Genetics|September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, 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.
Physical Review Letters|November 24, 2011
Evidence for separatrix formation and sustainment with steady inductive helicity injectionB S Victor, T R Jarboe, A C Hossack, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
Pageof 64

Showing results (591-600 of 636) with videos related to

Sort By:
Pageof 64
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|December 24, 1997
Imported yellow fever in a United States citizenJ M McFarland, L M Baddour, J E Nelson, et al.
Nature|December 6, 2013
Highly polarized light from stable ordered magnetic fields in GRB 120308AC G Mundell, D Kopač, D M Arnold, et al.
Journal of Medical Genetics|March 21, 1998
A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2)N J Lench, A F Markham, R F Mueller, et al.
Clinical Genetics|September 5, 2001
Haplotype analysis of the USH1D locus and genotype-phenotype correlationsX Z Liu, S H Blanton, M Bitner-Glindzicz, et al.
American Journal of Medical Genetics|May 26, 1999
Maternally inherited nonsyndromic hearing lossR A Friedman, Y Bykhovskaya, C M Sue, et al.
Human Genetics|September 12, 2000
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairmentK Verhoeven, T Fagerheim, S Prasad, et al.
Genomics|February 15, 1997
The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7qP Coucke, G Van Camp, O Demirhan, 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.
Physical Review Letters|November 24, 2011
Evidence for separatrix formation and sustainment with steady inductive helicity injectionB S Victor, T R Jarboe, A C Hossack, et al.
American Journal of Human Genetics|March 23, 2000
Genomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaM D Weston, J D Eudy, S Fujita, et al.
Pageof 64