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V C Sheffield

Showing results (111-120 of 153) with videos related to

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American Journal of Medical Genetics|July 13, 2001
Evidence supporting WNT2 as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
Genomics|July 20, 1999
The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23S W Gorman, N B Haider, U Grieshammer, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Human Molecular Genetics|October 1, 1995
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage mapsV C Sheffield, J L Weber, K H Buetow, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Human Molecular Genetics|September 1, 1997
Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpointR Y Walder, H Shalev, T M Brennan, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Pageof 16

Showing results (111-120 of 153) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics|July 13, 2001
Evidence supporting WNT2 as an autism susceptibility geneT H Wassink, J Piven, V J Vieland, et al.
American Journal of Human Genetics|September 29, 2000
Pitfalls in homozygosity mappingM G Miano, S G Jacobson, A Carothers, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 18, 2001
Variation of codons 1961 and 2177 of the Stargardt disease gene is not associated with age-related macular degenerationR H Guymer, E Héon, A J Lotery, et al.
Genomics|July 20, 1999
The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23S W Gorman, N B Haider, U Grieshammer, et al.
Investigative Ophthalmology & Visual Science|January 3, 2001
Evaluation of the myocilin (MYOC) glaucoma gene in monkey and human steroid-induced ocular hypertensionJ H Fingert, A F Clark, J E Craig, et al.
Human Molecular Genetics|October 1, 1995
Survey of trinucleotide repeats in the human genome: assessment of their utility as genetic markersJ M Gastier, J C Pulido, S Sunden, et al.
Human Molecular Genetics|October 1, 1995
A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage mapsV C Sheffield, J L Weber, K H Buetow, et al.
Nature Genetics|September 6, 2000
Mutations in MKKS cause Bardet-Biedl syndromeA M Slavotinek, E M Stone, K Mykytyn, et al.
Human Molecular Genetics|September 1, 1997
Familial hypomagnesemia maps to chromosome 9q, not to the X chromosome: genetic linkage mapping and analysis of a balanced translocation breakpointR Y Walder, H Shalev, T M Brennan, et al.
Nature Genetics|April 16, 1998
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.
Pageof 16