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Showing results (131-140 of 153) with videos related to

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Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Genome Research|March 7, 2001
Generation of a high-density rat EST mapT E Scheetz, M R Raymond, D Y Nishimura, et al.
Genomics|February 15, 1996
Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2S L Sunden, T Businga, J Beck, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Genome Research|November 3, 2001
Automated construction of high-density comparative maps between rat, human, and mouseA E Kwitek, P J Tonellato, D Chen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 10, 2001
Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve headA F Clark, K Kawase, S English-Wright, et al.
Pageof 16

Showing results (131-140 of 153) with videos related to

Sort By:
Pageof 16
Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.
American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|February 1, 1996
Linkage of autosomal dominant radial drusen (malattia leventinese) to chromosome 2p16-21E Héon, B Piguet, F Munier, et al.
Human Molecular Genetics|January 12, 2001
Non-secretion of mutant proteins of the glaucoma gene myocilin in cultured trabecular meshwork cells and in aqueous humorN Jacobson, M Andrews, A R Shepard, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001
Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.
Genome Research|March 7, 2001
Generation of a high-density rat EST mapT E Scheetz, M R Raymond, D Y Nishimura, et al.
Genomics|February 15, 1996
Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2S L Sunden, T Businga, J Beck, et al.
Human Mutation|May 26, 1998
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing lossD A Scott, M L Kraft, R Carmi, et al.
Genome Research|November 3, 2001
Automated construction of high-density comparative maps between rat, human, and mouseA E Kwitek, P J Tonellato, D Chen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|May 10, 2001
Expression of the glaucoma gene myocilin (MYOC) in the human optic nerve headA F Clark, K Kawase, S English-Wright, et al.
Pageof 16