Yildiz, D <br/><br/>
Crigler-Najjar syndrome type I in a Turkish newborn caused by a novel mutation and Gilbert type genetic defect.  [electronic resource] 

 -  Genetic counseling (Geneva, Switzerland)  2013 
 - 273-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1015-8146 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Consanguinity<br/>Crigler-Najjar Syndrome--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Gilbert Disease--genetics<br/>Glucuronosyltransferase--genetics<br/>Humans<br/>Infant, Newborn<br/>Mutation<br/>Phototherapy--methods<br/>Turkey