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Human Genetics|January 1, 1984
Familial benign hypercalcaemia (FBH; McK. No. 14598, 1983): linkage studies in a large Dutch familyF H Menko, O L Bijvoet, P Meera Khan, et al.Human Genetics|May 1, 1989
Family and population studies on the human pepsinogen A multigene familyJ P Bebelman, M P Evers, B Zelle, et al.Genomics|April 1, 1989
Nucleotide sequence comparison of five human pepsinogen A (PGA) genes: evolution of the PGA multigene familyM P Evers, B Zelle, J P Bebelman, et al.European Journal of Clinical Investigation|June 1, 1989
The glomerular sieving of pepsinogen A and C in manR W ten Kate, G Pals, J C Res, et al.Human Genetics|January 1, 1985
Assignment of human pepsinogen A locus to the q12-pter region of chromosome 11B Zelle, A Geurts van Kessel, J de Wit, et al.Human Genetics|January 1, 1988
Genomic structure and evolution of the human pepsinogen A multigene familyB Zelle, M P Evers, P C Groot, et al.Clinical Genetics|August 1, 1988
Differential expression of pepsinogen isozymogens in a patient with Barrett esophagusG Pals, A W Eriksson, J C Pronk, et al.American Journal of Human Genetics|October 23, 1997
Evidence for at least eight Fanconi anemia genesH Joenje, A B Oostra, M Wijker, et al.British Journal of Cancer|March 31, 1999
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3A M Cleton-Jansen, E W Moerland, J C Pronk, et al.European Journal of Human Genetics : EJHG|September 27, 2003
Anticipation in familial intracranial aneurysms in consecutive generationsP M Struycken, G Pals, M Limburg, et al.Pageof 7