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M Leppert

Showing results (301-310 of 315) with videos related to

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Cancer|September 1, 1992
Colon cancer geneticsH T Lynch, P Watson, T C Smyrk, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Journal of Glaucoma|December 1, 1996
A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucomaK L Anderson, R A Lewis, B A Bejjani, et al.
American Journal of Medical Genetics|December 18, 1998
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated familiesB K Goodman, L G Shaffer, J Rutberg, et al.
Blood|June 15, 1996
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2C Y Ho, B Otterud, R D Legare, et al.
Science (New York, N.Y.)|September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degenerationR Allikmets, N F Shroyer, N Singh, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 27, 2015
Transfontanellar duplex brain ultrasonography resistive indices as a prognostic tool in neonatal hypoxic-ischemic encephalopathy before and after treatment with therapeutic hypothermiaG J Gerner, V J Burton, A Poretti, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Neurology|July 26, 2000
Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studiesK J Swoboda, B Soong, C McKenna, et al.
Nature Genetics|March 1, 1997
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophyR Allikmets, N Singh, H Sun, et al.
Pageof 32

Showing results (301-310 of 315) with videos related to

Sort By:
Pageof 32
Cancer|September 1, 1992
Colon cancer geneticsH T Lynch, P Watson, T C Smyrk, et al.
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Journal of Glaucoma|December 1, 1996
A gene for primary congenital glaucoma is not linked to the locus on chromosome 1q for autosomal dominant juvenile-onset open angle glaucomaK L Anderson, R A Lewis, B A Bejjani, et al.
American Journal of Medical Genetics|December 18, 1998
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated familiesB K Goodman, L G Shaffer, J Rutberg, et al.
Blood|June 15, 1996
Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2C Y Ho, B Otterud, R D Legare, et al.
Science (New York, N.Y.)|September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degenerationR Allikmets, N F Shroyer, N Singh, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 27, 2015
Transfontanellar duplex brain ultrasonography resistive indices as a prognostic tool in neonatal hypoxic-ischemic encephalopathy before and after treatment with therapeutic hypothermiaG J Gerner, V J Burton, A Poretti, et al.
Nature Genetics|January 13, 1998
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newbornsN A Singh, C Charlier, D Stauffer, et al.
Neurology|July 26, 2000
Paroxysmal kinesigenic dyskinesia and infantile convulsions: clinical and linkage studiesK J Swoboda, B Soong, C McKenna, et al.
Nature Genetics|March 1, 1997
A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophyR Allikmets, N Singh, H Sun, et al.
Pageof 32