Anzahl der Einträge: 15.
Artikel
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
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.
Riess, O.,
Noerremoelle, A.,
Collins, C.,
Mah, D.,
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
und
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, S. 104-108.
Volltext nicht vorhanden.
Riess, O.,
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
Noerremoelle, A.,
Shaikh, R. A.,
Hayden, M. R. und
Musarella, M. A.
(1992)
Linkage studies and mutation analysis of the PDEB gene in 23 families with leber congenital amaurosis.
Human Mutation 1 (6), S. 478-485.
Volltext nicht vorhanden.
Andrew, S.,
Theilmann, J.,
Hedrick, A.,
Mah, D.,
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
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.
Collins, C.,
Hutchinson, G.,
Kowbel, D.,
Riess, O.,
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
und
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), S. 698-704.
Volltext nicht vorhanden.
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
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.
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
Allen, L.,
Magenis, R. E.,
Goodfellow, P. J.,
Smith, L. und
Hayden, M. R.
(1991)
Intrachromosomal location of the telomeric repeat (TTAGGG)n.
Mammalian Genome 1 (4), S. 211-216.
Volltext nicht vorhanden.
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
Collins, C.,
Robbins, C.,
Magenis, R. E.,
Delaney, A. D.,
Gray, J. W. und
Hayden, M. R.
(1990)
Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.
Nucleic Acids Research 18 (11), S. 3353-3361.
Theilmann, J.,
Kanani, S.,
Shiang, R.,
Robbins, C.,
Quarrell, O.,
Huggins, M.,
Hedrick, A.,
Weber, Bernhard H. F. ![ORCID 0000-0002-8808-7723](/images/orcid_16x16.gif)
,
Collins, C.,
Wasmuth, J. J.,
Buetow, K. H.,
Murray, J. C. und
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), S. 676-681.
Volltext nicht vorhanden.
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