Abstract
Genetic counselling in hereditary bleeding disorders mainly concerns haemophilia, since the other disorders i.e. thrombocytopathy of Glanzmann-Naegeli and the inherited coagulation-factor deficiencies of factors ii, v, vii, x, and xi are rare and show autosomal inheritance. Only homozygotes for these pathologic genes have a tendency to bleed, and genetic advice would be relevant only with respect to an intrafamilial marriage.
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Veltkamp, J. J., E. F. Drion, E. A. Loeliger, Detection of the carrier state in hereditary coagulation disorders. Thrombos. Diathes. haemorrh. I, 19, 479(1968), Thrombos.Diathes. haemorrh. II, 19, 403 (1968).
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© 1969 Leiden University Press, Leiden, The Netherlands
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Veltkamp, J.J. (1969). Genetic Counselling in Haemostatic Disorders. In: Hemker, H.C., Loeliger, E.A., Veltkamp, J.J. (eds) Human Blood Coagulation. Boerhaave Series for Postgraduate Medical Education, vol 1. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-3423-4_33
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DOI: https://doi.org/10.1007/978-94-010-3423-4_33
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