Sipahi, T <br/><br/>
Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence.  [electronic resource] 

 -  European journal of haematology  Apr 1999 
 - 281-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0902-4441 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0609.1999.tb01759.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Brain--pathology<br/>Cerebral Infarction--complications<br/>Cystic Fibrosis--complications<br/>Female<br/>Genetic Variation<br/>Humans<br/>Infant<br/>Magnetic Resonance Imaging<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Prothrombin--genetics<br/>Turkey