Xu, Yongbin <br/><br/>
[Analysis of genetic mutations and pathogenesis for two children with Omenn syndrome].  [electronic resource] 

 -  Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics  Feb 2016 
 - 38-43 p.  digital 
<br/><br/> Publication Type: Case Reports; English Abstract; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1003-9406 
<br/><br/><label>Standard No.: </label>10.3760/cma.j.issn.1003-9406.2016.01.010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Heterozygote<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Infant<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Nuclear Proteins--genetics<br/>Pedigree<br/>Severe Combined Immunodeficiency--genetics