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Human Genetics|July 18, 1979
Genetic variation in parotid basic proteins (Pb) in the Bozo (Mali, West Africa)G Pals, J C PronkHuman Genetics|September 10, 1976
Leukocyte peroxidase in Spielmeyer-Vogt's diseaseJ C Pronk, J F KosterHuman Heredity|January 1, 1988
Complement C4 phenotypes in dementia of the Alzheimer typeP Eikelenboom, J Goetz, J C Pronk, et al.Immunology|September 1, 1986
Production and characterization of pepsin fragments of human IgA1 to determine domain-specificity of monoclonal anti-IgA antibodiesJ Biewenga, A Faber, J C Pronk, et al.Acta Psychiatrica Scandinavica|February 1, 1984
C3 and haptoglobin polymorphism in dementia of the Alzheimer typeP Eikelenboom, M L Vink-Starreveld, W Jansen, et al.British Journal of Haematology|February 23, 1999
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous familyA Koc, J C Pronk, M Alikasifoglu, et al.Journal of Paediatrics and Child Health|January 27, 2005
Vanishing white matter disease in a child presenting with ataxiaC J Wilson, J C Pronk, M S Van der KnaapNederlands Tijdschrift Voor Geneeskunde|October 31, 2002
[From gene to disease; a defect in the regulation of protein production leading to vanishing white matter]J C Pronk, P A J Leegwater, M S van der KnaapPageof 7