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B M Ross

Showing results (51-60 of 58) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 15, 1993
Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene regionP W Kleyn, C H Wang, L L Lien, et al.
Archives of Neurology|October 21, 1998
Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disordersS J Kish, I Lopes-Cendes, M Guttman, et al.
Journal of Neurochemistry|May 9, 2000
The human nucleus accumbens is highly susceptible to G protein down-regulation by methamphetamine and heroinE R McLeman, J J Warsh, L Ang, et al.
Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.
Neurology|September 19, 2007
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson diseaseL N Clark, B M Ross, Y Wang, et al.
Human Molecular Genetics|February 1, 1997
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletionsT A Carter, C G Bönnemann, C H Wang, et al.
American Journal of Human Genetics|August 1, 1997
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analysesA B Shah, I Chernov, H T Zhang, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
Proceedings of the National Academy of Sciences of the United States of America|July 15, 1993
Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene regionP W Kleyn, C H Wang, L L Lien, et al.
Archives of Neurology|October 21, 1998
Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disordersS J Kish, I Lopes-Cendes, M Guttman, et al.
Journal of Neurochemistry|May 9, 2000
The human nucleus accumbens is highly susceptible to G protein down-regulation by methamphetamine and heroinE R McLeman, J J Warsh, L Ang, et al.
Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.
Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.
Neurology|September 19, 2007
Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson diseaseL N Clark, B M Ross, Y Wang, et al.
Human Molecular Genetics|February 1, 1997
A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletionsT A Carter, C G Bönnemann, C H Wang, et al.
American Journal of Human Genetics|August 1, 1997
Identification and analysis of mutations in the Wilson disease gene (ATP7B): population frequencies, genotype-phenotype correlation, and functional analysesA B Shah, I Chernov, H T Zhang, et al.
Pageof 6