Combination of congenital coagulation disorders: Factor II gene mutation G20210A, Factor V Leiden gene mutation G1691A and protein S deficiency. a family study. [electronic resource]

By: Contributor(s): Producer: 20040129Description: ECR20 p. digitalISSN:
  • 1592-8721
Subject(s): In: Haematologica vol. 88
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Publication Type: Journal Article

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