Renal embolisation in Glanzmann's thrombasthenia.

Bằng Briët, E, Vismans, F J, van Voorthuisen, A E
Được phát hành 1980

A Dutch family with moderately severe hemophilia B (factor IXHeerde) has a missense mutation identical to that of factor IX London 2.

Bằng Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Được phát hành 1989

A Dutch pedigree with mild hemophilia B with a missense mutation in the first EGF domain (factor IXOud en Nieuw Gastel).

Bằng Poort, S R, Briët, E, Bertina, R M, Reitsma, P H
Được phát hành 1989

RFLP for a human von Willebrand factor (vWF) cDNA clone, pvWF1100.

Bằng Verweij, C L, Hofker, M, Quadt, R, Briet, E, Pannekoek, H
Được phát hành 1985

Multiple substitutions in the von Willebrand factor gene that mimic the pseudogene sequence.

Bằng Eikenboom, J C, Vink, T, Briët, E, Sixma, J J, Reitsma, P H
Được phát hành 1994

A polymorphic Xba I site within the human von Willebrand factor (vWF) gene identified by a vWF cDNA clone.

Bằng Quadt, R, Verweij, C L, de Vries, C J, Briët, E, Pannekoek, H
Được phát hành 1986

Survival in families with hereditary protein C deficiency, 1820 to 1993.

Bằng Allaart, C. F., Rosendaal, F. R., Noteboom, W. M., Vandenbroucke, J. P., Briët, E.
Được phát hành 1995

Genetic linkage of two intragenic restriction fragment length polymorphisms with von Willebrand's disease type IIA. Evidence for a defect in the von Willebrand factor gene.

Bằng Verweij, C L, Quadt, R, Briët, E, Dubbeldam, K, van Ommen, G B, Pannekoek, H
Được phát hành 1988

Physical condition, longevity, and social performance of Dutch haemophiliacs, 1972-85.

Bằng Smit, C., Rosendaal, F. R., Varekamp, I., Bröcker-Vriends, A., Van Dijck, H., Suurmeijer, T. P., Briët, E.
Được phát hành 1989

Characterization of the clotting activities of structurally different forms of activated factor IX. Enzymatic properties of normal human factor IXa alpha, factor IXa beta, and acti...

Bằng Griffith, M J, Breitkreutz, L, Trapp, H, Briet, E, Noyes, C M, Lundblad, R L, Roberts, H R
Được phát hành 1985

Combined hereditary deficiency of the sixth component of complement and factor VIII coagulant activity in a Dutch family.

Bằng Daha, M R, Bertina, R M, Thompson, J, Kauffmann, R H, Nicholson-Weller, A, Veltkamp, J J, Briët, E
Được phát hành 1982

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

Bằng Deutz-Terlouw, P P, Losekoot, M, Olmer, R, Pieneman, W C, de Vries-v d Weerd, S, Briët, E, Bakker, E
Được phát hành 1995

Cerebral haemorrhagic infarction in young patients with hereditary protein C deficiency: evidence for "spontaneous" cerebral venous thrombosis.

Bằng Wintzen, A R, Broekmans, A W, Bertina, R M, Briët, E, Briët, P E, Zecha, A, Vielvoye, G J, Bots, G T
Được phát hành 1985

The human clotting factor VIII cDNA contains an autonomously replicating sequence consensus- and matrix attachment region-like sequence that binds a nuclear factor, represses heter...

Bằng Fallaux, F J, Hoeben, R C, Cramer, S J, van den Wollenberg, D J, Briët, E, van Ormondt, H, van Der Eb, A J
Được phát hành 1996

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis.

Bằng Bröcker-Vriends, A H, Rosendaal, F R, van Houwelingen, J C, Bakker, E, van Ommen, G J, van de Kamp, J J, Briët, E
Được phát hành 1991

Haemophilia: strategies for carrier detection and prenatal diagnosis.

Bằng Peake, I. R., Lillicrap, D. P., Boulyjenkov, V., Briet, E., Chan, V., Ginter, E. K., Kraus, E. M., Ljung, R., Mannucci, P. M., Nicolaides, K.
Được phát hành 1993