Margaglione, M <br/><br/>
Compound heterozygosity (554-589 del, C515-T transition) in the platelet glycoprotein Ib alpha gene in a patient with a severe bleeding tendency.  [electronic resource] 

 -  Thrombosis and haemostasis  Apr 1999 
 - 486-92 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6245 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Bernard-Soulier Syndrome--diagnosis<br/>Blood Platelets--chemistry<br/>Family Health<br/>Female<br/>Genetic Heterogeneity<br/>Humans<br/>Platelet Glycoprotein GPIb-IX Complex--genetics<br/>Polymorphism, Single-Stranded Conformational<br/>Sequence Analysis, DNA