ROSENBERG, N., HAUSCHNER, H., PERETZ, H., MOR-COHEN, R., LANDAU, M., SHENKMAN, B., . . . SELIGSOHN, U. (2005). A 13-bp deletion in α(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
Chicago Style citaatROSENBERG, N., et al. A 13-bp Deletion in α(IIb) Gene Is a Founder Mutation That Predominates in Palestinian-Arab Patients With Glanzmann Thrombasthenia. 2005.
MLA citatieROSENBERG, N., et al. A 13-bp Deletion in α(IIb) Gene Is a Founder Mutation That Predominates in Palestinian-Arab Patients With Glanzmann Thrombasthenia. 2005.
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