Okur, Ilyas <br/><br/>
Crisponi syndrome: a new case with additional features and new mutation in CRLF1.  [electronic resource] 

 -  American journal of medical genetics. Part A  Dec 2008 
 - 3237-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32531  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation--genetics<br/>Receptors, Cytokine--genetics<br/>Syndrome