Einträge von Andrew, S. auf dem Publikationsserver

Weber, Bernhard H. F. , Riess, O., Wolff, G., Andrew, S., Collins, C., Graham, R., Theilmann, J. und 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, S. 216-222. Volltext nicht vorhanden.

Weber, Bernhard H. F. , Hedrick, A., Andrew, S., Riess, O., Collins, C., Kowbel, D. und 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), S. 382-393. Volltext nicht vorhanden.

Andrew, S., Theilmann, J., Hedrick, A., Mah, D., Weber, Bernhard H. F. und Hayden, M. R. (1992) Nonrandom association between huntington disease and two loci separated by about 3 Mb on 4p16.3. Genomics 13 (2), S. 301-311. Volltext nicht vorhanden.

Weber, Bernhard H. F. , Riess, O., Hutchinson, G., Collins, C., Lin, B., Kowbel, D., Andrew, S., Schappert, K. und 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), S. 6263-6268.