P. Deutz‐Terlouw

发表

Rapid identification of IDH1 and IDH2 mutations in acute myeloid leukaemia using high resolution melting curve analysis

J. Jansen, S. M. Noordermeer, B. A. van der Reijden, 2011, British journal of haematology.

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

R. Bertina, A. van Wijngaarden, L. Ballering, 1990, Clinica chimica acta; international journal of clinical chemistry.

Eleven novel mutations in the factor VIII gene from Brazilian hemophilia A patients.

P. Reitsma, F. Costa, V. Arruda, 1995, Blood.

Inversions in the factor VIII gene: improvement of carrier detection and prenatal diagnosis in Dutch haemophilia A families.

E. Bakker, M. Losekoot, E. Briët, 1995, Journal of medical genetics.

Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.

P. Reitsma, R. Bertina, H. K. Ploos van Amstel, 1990, Blood.

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

B. de Geus, E. Bakker, J. Rozing, 1995, Journal of immunological methods.

Immunoradiometric assays for the Ca(II)-dependent and Ca(II)-independent conformation of human protein C.

R. Bertina, S. Poort, A. van Wijngaarden, 1988, Thrombosis research.

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

E. Bakker, J. Dunnen, G. Van, 1995, Human mutation.

Immunoradiometric Assay for the Calcium-Stabilized Conformation of Human Protein S

R. Bertina, S. Poort, A. van Wijngaarden, 1987, Thrombosis and Haemostasis.

Screening for mutations in haemophilia A patients by multiplex PCR‐SSCP, Southern blotting and RNA analysis: the detection of a genetic abnormality in the factor VIII gene in 30 out of 35 patients

P. Reitsma, E. Briet, W. C. Pieneman, 1995, British journal of haematology.

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

P. Reitsma, R. Bertina, P. A. van der Velden, 1990, Thrombosis and Haemostasis.

First‐trimester prenatal diagnosis in twin pregnancies

J. Oosterwijk, E. Bakker, R. Stigter, 1994, Prenatal diagnosis.

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

E. Bakker, R. Hennekam, M. Losekoot, 1998, Human mutation.