Chromosomes 14 and 21 as possible candidates for mapping the gene for Sanfilippo disease type IIIC.

Por Zaremba, J, Kleijer, W J, Huijmans, J G, Poorthuis, B, Fidzianska, E, Glogowska, I
Publicado em 1992

Prenatal diagnosis of genetic disorders.

Por Niermeijer, M F, Sachs, E S, Jahodova, M, Tichelaar-Klepper, C, Kleijer, W J, Galjaard, H
Publicado em 1976

Fibroblast silver loading for the diagnosis of Menkes disease.

Por Verheijen, F W, Beerens, C E, Havelaar, A C, Kleijer, W J, Mancini, G M
Publicado em 1998

Clinical heterogeneity and novel mutations in the glycerol kinase gene in three families with isolated glycerol kinase deficiency.

Por Sjarif, D R, Sinke, R J, Duran, M, Beemer, F A, Kleijer, W J, Ploos van Amstel, J K, Poll-The, B T
Publicado em 1998

Xeroderma pigmentosum--Cockayne syndrome complex: a further case.

Por Hamel, B C, Raams, A, Schuitema-Dijkstra, A R, Simons, P, van der Burgt, I, Jaspers, N G, Kleijer, W J
Publicado em 1996

Coexistence of Gaucher disease type 1 and Joubert syndrome.

Por van Royen-Kerkhof, A, Poll-The, B T, Kleijer, W J, van Diggelen, O P, Aerts, J M, Hopwood, J J, Beemer, F A
Publicado em 1998

Molecular analysis of patients with beta-glucuronidase deficiency presenting as hydrops fetalis or as early mucopolysaccharidosis VII.

Por Vervoort, R., Islam, M. R., Sly, W. S., Zabot, M. T., Kleijer, W. J., Chabas, A., Fensom, A., Young, E. P., Liebaers, I., Lissens, W.
Publicado em 1996

Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.

Por Vermeulen, W., Scott, R. J., Rodgers, S., Müller, H. J., Cole, J., Arlett, C. F., Kleijer, W. J., Bootsma, D., Hoeijmakers, J. H., Weeda, G.
Publicado em 1994

Spectrum of mutations in the gene encoding the adrenoleukodystrophy protein.

Por Ligtenberg, M J, Kemp, S, Sarde, C O, van Geel, B M, Kleijer, W J, Barth, P G, Mandel, J L, van Oost, B A, Bolhuis, P A
Publicado em 1995

Glycogen storage disease type II: frequency of three common mutant alleles and their associated clinical phenotypes studied in 121 patients.

Por Kroos, M A, Van der Kraan, M, Van Diggelen, O P, Kleijer, W J, Reuser, A J, Van den Boogaard, M J, Ausems, M G, Ploos van Amstel, H K, Poenaru, L, Nicolino, M
Publicado em 1995