Sipahi, T <br/><br/>
Compound heterozygosity for factor V Leiden and prothrombin G20210A mutations in a child with Budd-Chiari syndrome.  [electronic resource] 

 -  European journal of pediatrics  Mar 2001 
 - 198 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/pl00008425  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Budd-Chiari Syndrome--genetics<br/>Child<br/>Factor V--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Mutation<br/>Prothrombin--genetics