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February 1 1990
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ARTICLES
Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual
IR Peake,MB Liddell,P Moodie,G Standen,DJ Mancuso,EA Tuley,LA Westfield,JM Sorace,JE Sadler,CL Verweij
RANDOMIZED CONTROLLED TRIAL
CORRESPONDENCE
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