Piëtte P. Deutz-Terlouw

Asn540Thr substitution in the fibroblast growth factor receptor 3 tyrosine kinase domain causing hypochondroplasia

Piëtte P. Deutz-Terlouw, Monique Losekoot, Cora M. Aalfs et al. · Human Mutation · 1998 · 52 citations

Life Sciences, Genetics, Molecular Biology +11

Two ELISA's for measurement of protein S, and their use in the laboratory diagnosis of protein S deficiency

Piëtte P. Deutz-Terlouw, Leo Ballering, A van Wijngaarden et al. · Clinica Chimica Acta · 1990 · 35 citations

Life Sciences, Biochemistry, Molecular Biology +11

Point mutation screening for 16 exons of the dystrophin gene by multiplex single-strand conformation polymorphism analysis

Alexander L.J. Kneppers, Piëtte P. Deutz-Terlouw, Johan T. den Dunnen et al. · Human Mutation · 1995 · 26 citations

Life Sciences, Genetics, Molecular Genetics +17

Denaturing and non-denaturing gel electrophoresis as methods for the detection of junctional diversity in rearranged T cell receptor sequences

Myriam T.C. Offermans, Renate D. Sonneveld, E.H. Bakker et al. · Journal of Immunological Methods · 1995 · 11 citations

Life Sciences, Immunology, Molecular Biology +16

Application of Two Neutral Mspl DNA Polymorphisms in the Analysis of Hereditary Protein C Deficiency

P H Reitsma, W. te Lintel Hekkert, E. Koenhen et al. · Thrombosis and Haemostasis · 1990 · 11 citations

Life Sciences, Genetics, Molecular Genetics +13