Gruber, Tanja A <br/><br/>
Clinical and genetic heterogeneity in Omenn syndrome and severe combined immune deficiency.  [electronic resource] 

 -  Pediatric transplantation  Mar 2009 
 - 244-50 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1399-3046 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-3046.2008.00970.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cytokines--genetics<br/>Exanthema--genetics<br/>Female<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Immunologic Deficiency Syndromes--complications<br/>Infant<br/>Male<br/>Models, Genetic<br/>Mutation<br/>Phenotype<br/>Severe Combined Immunodeficiency--complications<br/>T-Lymphocytes--metabolism<br/>Time Factors<br/>Treatment Outcome<br/>VDJ Recombinases--genetics