Magna Van der Kraan

Prevalent mutations in the GALC gene of patients with Krabbe disease of Dutch and other European origin

Wim J. Kleijer, J. L. M. Keulemans, Magna Van der Kraan et al. · Journal of Inherited Metabolic Disease · 1997 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +7

Prenatal Diagnosis of Glycogen Storage Disease Type II: Enzyme Assay or Mutation Analysis?

Wim J. Kleijer, Magna Van der Kraan, Marian A. Kroos et al. · Pediatric Research · 1995 · 32 citations

Life Sciences, Genetics, Molecular Genetics +16

Two extremes of the clinical spectrum of glycogen storage disease type II in one family: A matter of genotype

Marian A. Kroos, Magna Van der Kraan, Otto P. van Diggelen et al. · Human Mutation · 1997 · 23 citations

Life Sciences, Genetics, Molecular Genetics +17

Prenatal Diagnosis of Ataxia-telangiectasia and Nijmegen Breakage Syndrome by the Assay of Radioresistant DNA Synthesis

Wim J. Kleijer, Magna Van der Kraan, Frans J. Los et al. · International Journal of Radiation Biology · 1994 · 18 citations

Life Sciences, Genetics, Molecular Biology +8

First‐trimester prenatal diagnosis of the nijmegen breakage syndrome and ataxia telangiectasia using an assay of radioresistant dna synthesis

Nicolaas G.J. Jaspers, Magna Van der Kraan, P. Linssen et al. · Prenatal Diagnosis · 1990 · 17 citations

Life Sciences, Genetics, Molecular Genetics +14