Go to content
UR Home

Publications by Collins, C.

Up a level
Export as
[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item type | No Grouping
Number of items: 9.

Weber, Bernhard H. F. , Riess, O., Wolff, G., Andrew, S., Collins, C., Graham, R., Theilman, 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.

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.

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.

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.

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.

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.

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.

This list was generated on Wed May 12 22:55:37 2021 CEST.
  1. Homepage UR

University Library

Publication Server

Contact:

Publishing: oa@ur.de

Dissertations: dissertationen@ur.de

Research data: daten@ur.de

Contact persons