Conroy, J M <br/><br/>
The allele frequency of mutations in four genes that confer enhanced susceptibility to venous thromboembolism in an unselected group of New York State newborns.  [electronic resource] 

 -  Thrombosis research  Aug 2000 
 - 317-24 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0049-3848 
<br/><br/><label>Standard No.: </label>10.1016/s0049-3848(00)00254-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase--genetics<br/>Gene Frequency--genetics<br/>Genetic Predisposition to Disease<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant, Newborn--blood<br/>Methylenetetrahydrofolate Reductase (NADPH2)<br/>Mutation--genetics<br/>New York--epidemiology<br/>Oxidoreductases Acting on CH-NH Group Donors--genetics<br/>Prothrombin--genetics<br/>Racial Groups--genetics<br/>Thromboembolism--ethnology<br/>Venous Thrombosis--ethnology