Identification of the most common mutation within the porphobilinogen deaminase gene in Swedish patients with acute intermittent porphyria.

Por Lee, J S, Anvret, M
Publicado em 1991

A PstI polymorphism for the human porphobilinogen deaminase gene (PBG).

Por Lee, J S, Anvret, M
Publicado em 1987

PstI RFLP for the anonymous [D13S2] (p9D11) probe.

Por Lee, J S, Anvret, M
Publicado em 1989

An EcoRI polymorphism of the human von Willebrand factor cDNA (VWF).

Por Lindstedt, M, Anvret, M
Publicado em 1989

An EcoRI polymorphism of the human von Willebrand factor cDNA (VWF).

Por Lindstedt, M, Anvret, M
Publicado em 1989

Integrated viral DNA sequences in Epstein-Barr virus-converted human lymphoma lines.

Por Andersson-Anvret, M, Lindahl, T
Publicado em 1978

Evidence for integrated EBV genomes in Raji cellular DNA.

Por Anvret, M, Karlsson, A, Bjursell, G
Publicado em 1984

Mutations of von Willebrand factor gene in families with von Willebrand disease in the Aland Islands.

Por Zhang, Z P, Blombäck, M, Nyman, D, Anvret, M
Publicado em 1993

Mutation screening in Rett syndrome patients

Por Xiang, F., Buervenich, S., Nicolao, P., Bailey, M., Zhang, Z., Anvret, M.
Publicado em 2000

Nonsense mutations of the von Willebrand factor gene in patients with von Willebrand disease type III and type I.

Por Zhang, Z P, Lindstedt, M, Falk, G, Blombäck, M, Egberg, N, Anvret, M
Publicado em 1992

Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q.

Por Nicolao, P, Xiang, F, Gunnarsson, L G, Giometto, B, Edström, L, Anvret, M, Zhang, Z
Publicado em 1999

Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria.

Por Lundin, G, Hashemi, J, Floderus, Y, Thunell, S, Sagen, E, Laegreid, A, Wassif, W, Peters, T, Anvret, M
Publicado em 1995

Imprinting mutations suggested by abnormal DNA methylation patterns in familial Angelman and Prader-Willi syndromes.

Por Reis, A., Dittrich, B., Greger, V., Buiting, K., Lalande, M., Gillessen-Kaesbach, G., Anvret, M., Horsthemke, B.
Publicado em 1994

A Huntington disease-like neurodegenerative disorder maps to chromosome 20p.

Por Xiang, F, Almqvist, E W, Huq, M, Lundin, A, Hayden, M R, Edström, L, Anvret, M, Zhang, Z
Publicado em 1998

Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasia.

Por Saemundsen, A K, Berkel, A I, Henle, W, Henle, G, Anvret, M, Sanal, O, Ersoy, F, Cağlar, M, Klein, G
Publicado em 1981

Chromosome mapping of Rett syndrome: a likely candidate region on the telomere of Xq.

Por Xiang, F, Zhang, Z, Clarke, A, Joseluiz, P, Sakkubai, N, Sarojini, B, Delozier-Blanchet, C D, Hansmann, I, Edström, L, Anvret, M
Publicado em 1998

Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Por Ellison, K A, Fill, C P, Terwilliger, J, DeGennaro, L J, Martin-Gallardo, A, Anvret, M, Percy, A K, Ott, J, Zoghbi, H
Publicado em 1992

Segregation of a totally skewed pattern of X chromosome inactivation in four familial cases of Rett syndrome without MECP2 mutation: implications for the disease

Por Villard, L., Levy, N., Xiang, F., Kpebe, A., Labelle, V., Chevillard, C., Zhang, Z., Schwartz, C., Tardieu, M., Chelly, J., Anvret, M., Fontes, M.
Publicado em 2001

Epstein-Barr virus in nasopharyngeal and salivary gland carcinomas of Greenland Eskimoes.

Por Saemundsen, A. K., Albeck, H., Hansen, J. P., Nielsen, N. H., Anvret, M., Henle, W., Henle, G., Thomsen, K. A., Kristensen, H. K., Klein, G.
Publicado em 1982

A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus

Por Johnson, K., Shelbourne, P., Davies, J., Buxton, J., Nimmo, E., Siciliano, M. J., Bachinski, L. L., Anvret, M., Harley, H., Rundle, S., Miki, T., Brunner, H., Williamson, R.
Publicado em 1990