T. Okamura

Inhibitory anti-factor V antibodies bind to the factor V C2 domain and are associated with hemorrhagic manifestations.

T. Ortel, M. Quinn-Allen, W. Kane, 1998, Blood.

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

Toshihiro Tanaka, H. Saito, Y. Nakamura, 2001, Blood.

Sibs with tetrasomy 18p born to a mother with trisomy 18p.

T. Hasegawa, K. Takeda, T. Okamura, 1989, Journal of medical genetics.

Genetic analysis of protein C deficiency in nineteen Japanese families: five recurrent defects can explain half of the deficiencies.

T. Miyata, A. Shirahata, H. Kato, 1998, Thrombosis research.

Sibswithtetrasomy 18pborntoamotherwithtrisomy 18p

K. Takeda, T. Okamura, 1988 .