Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.

Por Ho, M F, Monaco, A P, Blonden, L A, van Ommen, G J, Affara, N A, Ferguson-Smith, M A, Lehrach, H
Publicado em 1992

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

Por Blonden, L A, den Dunnen, J T, van Paassen, H M, Wapenaar, M C, Grootscholten, P M, Ginjaar, H B, Bakker, E, Pearson, P L, van Ommen, G J
Publicado em 1989

Chromosomal jumping from the DXS165 locus allows molecular characterization of four microdeletions and a de novo chromosome X/13 translocation associated with choroideremia.

Por Cremers, F P, van de Pol, D J, Wieringa, B, Collins, F S, Sankila, E M, Siu, V M, Flintoff, W F, Brunsmann, F, Blonden, L A, Ropers, H H
Publicado em 1989

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Por Den Dunnen, J T, Grootscholten, P M, Bakker, E, Blonden, L A, Ginjaar, H B, Wapenaar, M C, van Paassen, H M, van Broeckhoven, C, Pearson, P L, van Ommen, G J
Publicado em 1989

The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion

Por Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., de la Chapelle, A., Kiuru, A., Savontaus, M.-L., Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J.-C., Covone, A. E., Archidiacono, N., Romeo, G., Liechti-Gallati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, P., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., van Paassen, H. M. B., van Ommen, G. J. B., Kunkel, L. M.
Publicado em 1989