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J M Rapaport

Showing results (1-10 of 13) with videos related to

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Human Genetics|September 1, 1997
Quantification of the paternal allele bias for new germline mutations in the retinoblastoma geneT P Dryja, J F Morrow, J M Rapaport
Human Genetics|January 1, 1984
Chromosome 13 restriction fragment length polymorphismsT P Dryja, J M Rapaport, R Weichselbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomasT P Dryja, J M Rapaport, J M Joyce, et al.
American Journal of Ophthalmology|June 1, 1984
Linkage of genes for human esterase D and hereditary retinoblastomaS Mukai, J M Rapaport, J A Shields, et al.
American Journal of Human Genetics|May 1, 1991
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneT Sakai, J Toguchida, N Ohtani, et al.
Nature|June 15, 1989
Parental origin of mutations of the retinoblastoma geneT P Dryja, S Mukai, R Petersen, et al.
The New England Journal of Medicine|March 1, 1984
Homozygosity of chromosome 13 in retinoblastomaT P Dryja, W Cavenee, R White, et al.
American Journal of Human Genetics|January 1, 1986
Chromosome 13 homozygosity in osteosarcoma without retinoblastomaT P Dryja, J M Rapaport, J Epstein, et al.
Nature|October 16, 1986
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaS H Friend, R Bernards, S Rogelj, et al.
Human Genetics|January 1, 1983
Low incidence of deletion of the esterase D locus in retinoblastoma patientsT P Dryja, G A Bruns, B Gallie, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Human Genetics|September 1, 1997
Quantification of the paternal allele bias for new germline mutations in the retinoblastoma geneT P Dryja, J F Morrow, J M Rapaport
Human Genetics|January 1, 1984
Chromosome 13 restriction fragment length polymorphismsT P Dryja, J M Rapaport, R Weichselbaum, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1986
Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomasT P Dryja, J M Rapaport, J M Joyce, et al.
American Journal of Ophthalmology|June 1, 1984
Linkage of genes for human esterase D and hereditary retinoblastomaS Mukai, J M Rapaport, J A Shields, et al.
American Journal of Human Genetics|May 1, 1991
Allele-specific hypermethylation of the retinoblastoma tumor-suppressor geneT Sakai, J Toguchida, N Ohtani, et al.
Nature|June 15, 1989
Parental origin of mutations of the retinoblastoma geneT P Dryja, S Mukai, R Petersen, et al.
The New England Journal of Medicine|March 1, 1984
Homozygosity of chromosome 13 in retinoblastomaT P Dryja, W Cavenee, R White, et al.
American Journal of Human Genetics|January 1, 1986
Chromosome 13 homozygosity in osteosarcoma without retinoblastomaT P Dryja, J M Rapaport, J Epstein, et al.
Nature|October 16, 1986
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcomaS H Friend, R Bernards, S Rogelj, et al.
Human Genetics|January 1, 1983
Low incidence of deletion of the esterase D locus in retinoblastoma patientsT P Dryja, G A Bruns, B Gallie, et al.
Pageof 2