Trifa, Adrian P <br/><br/>
TERT rs2736100 A>C SNP and JAK2 46/1 haplotype significantly contribute to the occurrence of JAK2 V617F and CALR mutated myeloproliferative neoplasms - a multicentric study on 529 patients.  [electronic resource] 

 -  British journal of haematology  07 2016 
 - 218-26 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-2141 
<br/><br/><label>Standard No.: </label>10.1111/bjh.14041  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Calreticulin--genetics<br/>Case-Control Studies<br/>Female<br/>Genetic Predisposition to Disease<br/>Haplotypes--genetics<br/>Humans<br/>Janus Kinase 2--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Myeloproliferative Disorders--genetics<br/>Phenotype<br/>Polycythemia Vera--genetics<br/>Polymorphism, Single Nucleotide<br/>Primary Myelofibrosis--genetics<br/>Telomerase--genetics<br/>Thrombocythemia, Essential--genetics<br/>Young Adult