Geurts, J M <br/><br/>
Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia.  [electronic resource] 

 -  Human molecular genetics  Sep 2000 
 - 2067-74 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/9.14.2067  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Apolipoproteins B--biosynthesis<br/>Case-Control Studies<br/>Chromosomes, Human, Pair 1<br/>DNA Mutational Analysis<br/>Exons<br/>Family Health<br/>Female<br/>Genetic Linkage<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Hyperlipidemia, Familial Combined--blood<br/>Introns<br/>Linear Models<br/>Linkage Disequilibrium<br/>Male<br/>Middle Aged<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Receptors, Tumor Necrosis Factor--blood<br/>Receptors, Tumor Necrosis Factor, Type II<br/>Tumor Necrosis Factor-alpha