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The thrombocytopenia of Wiskott Aldrich syndrome is not related to a defect in proplatelet formation.

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Development of fluorine-18-labeled 5-HT1A antagonists.

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Regulation and function of WASp in platelets by the collagen receptor, glycoprotein VI.

Retrovirus-mediated WASP gene transfer corrects defective actin polymerization in B cell lines from Wiskott-Aldrich syndrome patients carrying 'null' mutations.

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