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Publications by Collins, C

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Jump to: 1992 | 1991 | 1989
Number of items: 7.


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. , 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.


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.

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