1. Acrofacial dysostosis in a patient with the TSC2-PKD1 contiguous gene syndrome. Issue 2 (1st February 2002) Authors: Dauwerse, J G; Bouman, K; van Essen, A J; van der Hout, A H; Kolsters, G; Breuning, M H; Peters, D J M Journal: Journal of medical genetics Issue: Volume 39:Issue 2(2002) Page Start: 136 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Heterozygous truncating mutation in the human homeobox gene GSH2 has no discernable phenotypic effect. Issue 9 (1st September 2002) Authors: Dauwerse, J G; de Die-Smulders, C E M; Bakker, E; Breuning, M H; Peters, D J M Journal: Journal of medical genetics Issue: Volume 39:Issue 9(2002) Page Start: 686 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1). Issue 10 (October 1990) Authors: Breuning, M H; Snijdewint, F G; Brunner, H; Verwest, A; Ijdo, J W; Saris, J J; Dauwerse, J G; Blonden, L; Keith, T; Callen, D F Journal: Journal of medical genetics Issue: Volume 27:Issue 10(1990) Page Start: 603 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene. Issue 10 (October 1990) Authors: Breuning, M H; Snijdewint, F G; Dauwerse, J G; Saris, J J; Bakker, E; Pearson, P L; vanOmmen, G J Journal: Journal of medical genetics Issue: Volume 27:Issue 10(1990) Page Start: 614 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗