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Entries of Collins, C. on the publication server
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Number of items: 9.
1992
Weber, Bernhard H. F. 
, Riess, O., Wolff, G., Andrew, S., Collins, C., Graham, R., Theilmann, J. and Hayden, M. R.
(1992)
Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease.
Nature Genetics 2, pp. 216-222.
Fulltext not available.
, Riess, O., Wolff, G., Andrew, S., Collins, C., Graham, R., Theilmann, J. and Hayden, M. R.
(1992)
Delineation of a 50 kilobase DNA segment containing the recombination site in a sporadic case of Huntington's disease.
Nature Genetics 2, pp. 216-222.
Fulltext not available.
Riess, O., Noerremoelle, A., Collins, C., Mah, D., Weber, Bernhard H. F. and Hayden, M. R.
(1992)
Exclusion of DNA changes in the bold beta−subunit of the c−GMP phosphodiesterase gene as the cause for Huntington's disease.
Nature Genetics 1, pp. 104-108.
Fulltext not available.
and Hayden, M. R.
(1992)
Exclusion of DNA changes in the bold beta−subunit of the c−GMP phosphodiesterase gene as the cause for Huntington's disease.
Nature Genetics 1, pp. 104-108.
Fulltext not available.
Weber, Bernhard H. F. , Hedrick, A., Andrew, S., Riess, O., Collins, C., Kowbel, D. and Hayden, M.
(1992)
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.
The American Journal of Human Genetics 50 (2), pp. 382-393.
Fulltext not available.
, Hedrick, A., Andrew, S., Riess, O., Collins, C., Kowbel, D. and Hayden, M.
(1992)
Isolation and characterization of new highly polymorphic DNA markers from the Huntington disease region.
The American Journal of Human Genetics 50 (2), pp. 382-393.
Fulltext not available.
Collins, C., Hutchinson, G., Kowbel, D., Riess, O., Weber, Bernhard H. F. and Hayden, M. R.
(1992)
The human β-subunit of rod photoreceptor cGMP phosphodiesterase: Complete retinal cDNA sequence and evidence for expression in brain.
Genomics 13 (3), pp. 698-704.
Fulltext not available.
and Hayden, M. R.
(1992)
The human β-subunit of rod photoreceptor cGMP phosphodiesterase: Complete retinal cDNA sequence and evidence for expression in brain.
Genomics 13 (3), pp. 698-704.
Fulltext not available.
1991
Weber, Bernhard H. F. , Riess, O., Hutchinson, G., Collins, C., Lin, B., Kowbel, D., Andrew, S., Schappert, K. and Hayden, M. R.
(1991)
Genomic organization and complete sequence of the human gene encoding the β-subunit of the cGMP phosphodiesterase and its localisation to 4p16.3.
Nucleic Acids Research 19 (22), pp. 6263-6268.
Weber, Bernhard H. F. , Collins, C., Kowbel, D., Riess, O. and Hayden, M. R.
(1991)
Identification of multiple CpG-islands and associated conserved sequences in a candidate region for the Huntington Disease gene.
Genomics 11 (4), pp. 1113-1124.
Fulltext not available.
, Collins, C., Kowbel, D., Riess, O. and Hayden, M. R.
(1991)
Identification of multiple CpG-islands and associated conserved sequences in a candidate region for the Huntington Disease gene.
Genomics 11 (4), pp. 1113-1124.
Fulltext not available.
Adam, S., Theilmann, J., Buetow, K., Hedrick, A., Collins, C., Weber, Bernhard H. F. , Huggins, M. and Hayden, M.
(1991)
Linkage disequilibrium and modification of risk for Huntington disease.
The American Journal of Human Genetics 48 (3), pp. 595-603.
Fulltext not available.
, Huggins, M. and Hayden, M.
(1991)
Linkage disequilibrium and modification of risk for Huntington disease.
The American Journal of Human Genetics 48 (3), pp. 595-603.
Fulltext not available.
1990
Weber, Bernhard H. F. , Collins, C., Robbins, C., Magenis, R. E., Delaney, A. D., Gray, J. W. and Hayden, M. R.
(1990)
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.
Nucleic Acids Research 18 (11), pp. 3353-3361.
1989
Theilmann, J., Kanani, S., Shiang, R., Robbins, C., Quarrell, O., Huggins, M., Hedrick, A., Weber, Bernhard H. F. , Collins, C., Wasmuth, J. J., Buetow, K. H., Murray, J. C. and Hayden, M. R.
(1989)
Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.
Journal of Medical Genetics 26 (11), pp. 676-681.
Fulltext not available.
, Collins, C., Wasmuth, J. J., Buetow, K. H., Murray, J. C. and Hayden, M. R.
(1989)
Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene.
Journal of Medical Genetics 26 (11), pp. 676-681.
Fulltext not available.
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