Herrmann, F H <br/><br/>
Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  Sep 2006 
 - 479-89 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1351-8216 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2516.2006.01303.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Child<br/>Child, Preschool<br/>Costa Rica--epidemiology<br/>Epistaxis--epidemiology<br/>Europe--epidemiology<br/>Factor X--genetics<br/>Factor X Deficiency--congenital<br/>Female<br/>Hemarthrosis--epidemiology<br/>Hematoma--epidemiology<br/>Hemorrhage--epidemiology<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Phenotype<br/>Prevalence<br/>Venezuela--epidemiology