Li, Xin <br/><br/>
Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants.  [electronic resource] 

 -  American journal of human genetics  Sep 2014 
 - 245-56 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2014.08.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Family<br/>Genome, Human<br/>Haplotypes--genetics<br/>High-Throughput Nucleotide Sequencing<br/>Humans<br/>Lymphocytes--metabolism<br/>Polymorphism, Single Nucleotide--genetics<br/>Quantitative Trait Loci<br/>RNA, Untranslated--genetics<br/>Sequence Analysis, RNA<br/>Transcriptome<br/>White People--genetics