Combes, Patricia <br/><br/>
Relevance of SOX17 variants for hypomyelinating leukodystrophies and congenital anomalies of the kidney and urinary tract (CAKUT).  [electronic resource] 

 -  Annals of human genetics  May 2012 
 - 261-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1469-1809 
<br/><br/><label>Standard No.: </label>10.1111/j.1469-1809.2011.00702.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Female<br/>Genetic Variation<br/>Hereditary Central Nervous System Demyelinating Diseases--genetics<br/>Humans<br/>Kidney--abnormalities<br/>Male<br/>SOXF Transcription Factors--genetics<br/>Urinary Tract--abnormalities