Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Por Bakker, E, Veenema, H, Den Dunnen, J T, van Broeckhoven, C, Grootscholten, P M, Bonten, E J, van Ommen, G J, Pearson, P L
Publicado em 1989

Apparent gene conversions involving the SMN gene in the region of the spinal muscular atrophy locus on chromosome 5.

Por van der Steege, G., Grootscholten, P. M., Cobben, J. M., Zappata, S., Scheffer, H., den Dunnen, J. T., van Ommen, G. J., Brahe, C., Buys, C. H.
Publicado em 1996

A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect

Por Rump, P., Lemmink, H. H., Verschuuren-Bemelmans, C. C., Grootscholten, P. M., Vos, Y. J., van Essen, A. J., Fock, J. M., Hayflick, S. J., Westaway, S. K.
Publicado em 2005

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

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