Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.

Por Hauksdóttir, H, Halldórsson, S, Jensson, O, Mikkelsen, M, McDermott, A
Publicado em 1972

A deleted B chromosome in a mosaic mother and her cri du chat progeny.

Por Philip, J, Brandt, N J, Friis-Hansen, B, Mikkelsen, M, Tygstrup, I
Publicado em 1970

Pericentric inversion of chromosome 13.

Por Hauksdóttir, H, Arnardóttir, A, Steinarsdóttir, M, Gudmundsdóttir, E, Halldórsson, S, Gunnarsson, A, Mikkelsen, M
Publicado em 1983

Significant increase in trisomy 21 in Berlin nine months after the Chernobyl reactor accident: temporal correlation or causal relation?

Por Sperling, K., Pelz, J., Wegner, R. D., Dörries, A., Grüters, A., Mikkelsen, M.
Publicado em 1994

Fallout from Chernobyl. Authors stand by study that Chernobyl increased trisomy 21 in Berlin.

Por Sperling, K., Pelz, J., Wegner, R. D., Dörries, A., Grüters, A., Mikkelsen, M.
Publicado em 1994

Ring chromosome 13: lack of distinct syndromes based on different breakpoints on 13q.

Por Brandt, C A, Hertz, J M, Petersen, M B, Vogel, F, Noer, H, Mikkelsen, M
Publicado em 1992

Investigation of a cluster of children with Down's syndrome born to mothers who had attended a school in Dundalk, Ireland

Por Dean, G, Nevin, N, Mikkelsen, M, Karadima, G, Petersen, M, Kelly, M, O'Sullivan, J
Publicado em 2000

Chemical cross-linking with thiol-cleavable reagents combined with differential mass spectrometric peptide mapping--a novel approach to assess intermolecular protein contacts.

Por Bennett, K. L., Kussmann, M., Björk, P., Godzwon, M., Mikkelsen, M., Sørensen, P., Roepstorff, P.
Publicado em 2000

"Compensatory" uniparental disomy of chromosome 21 in two cases.

Por Bartsch, O, Petersen, M B, Stuhlmann, I, Mau, G, Frantzen, M, Schwinger, E, Antonarakis, S E, Mikkelsen, M
Publicado em 1994

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome.

Por Petersen, M B, Schinzel, A A, Binkert, F, Tranebjaerg, L, Mikkelsen, M, Collins, F A, Economou, E P, Antonarakis, S E
Publicado em 1991

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Por Cremers, F P, van de Pol, T J, Wieringa, B, Hofker, M H, Pearson, P L, Pfeiffer, R A, Mikkelsen, M, Tabor, A, Ropers, H H
Publicado em 1988

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21

Por McGinniss, M. J., Kazazian, H. H., Stetten, G., Petersen, M. B., Boman, H., Engel, E., Greenberg, F., Hertz, J. M., Johnson, A., Laca, Z., Mikkelsen, M., Patil, S. R., Schinzel, A. A., Tranebjaerg, L., Antonarakis, S. E.
Publicado em 1992

Trisomy 21: Association between reduced recombination and nondisjunction

Por Sherman, S. L., Takaesu, N., Freeman, S. B., Grantham, M., Phillips, C., Blackston, R. D., Jacobs, P. A., Cockwell, A. E., Freeman, V., Uchida, I., Mikkelsen, M., Kurnit, D. M., Buraczynska, M., Keats, B. J. B., Hassold, T. J.
Publicado em 1991