Detection of the Carrier State in Hereditary Coagulation Disorders I

Please copy the URL and add it into your RSS Feed Reader.

Thromb Haemost 1968; 19(01/02): 279-303
DOI: 10.1055/s-0038-1651206

Originalarbeiten – Original Articles – Travaux Originaux

Schattauer GmbH

Detection of the Carrier State in Hereditary Coagulation Disorders^[*] I

J. J Veltkamp

¹Clinic for Internal Medicine of the University of Leyden (Prof. J. deGraeff M. D.) Department for Haemostasis and Thrombosis Research and the Statistical Department T. N. O, The Hague
E. F Drion

¹Clinic for Internal Medicine of the University of Leyden (Prof. J. deGraeff M. D.) Department for Haemostasis and Thrombosis Research and the Statistical Department T. N. O, The Hague
E. A Loeliger

¹Clinic for Internal Medicine of the University of Leyden (Prof. J. deGraeff M. D.) Department for Haemostasis and Thrombosis Research and the Statistical Department T. N. O, The Hague

Publication Date:
27 June 2018 (online)

^* Supported by a Grant from Stichting “De Drie Lichten”, Hilversum, the Netherlands.