Kucharczyk, Marzena <br/><br/>
Oculocutaneous albinism in a patient with 17p13.2-pter duplication - a review on the molecular syndromology of 17p13 duplication.  [electronic resource] 

 -  Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia  Jun 2015 
 - 333-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1804-7521 
<br/><br/><label>Standard No.: </label>10.5507/bp.2015.003  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Albinism, Oculocutaneous--genetics<br/>Child, Preschool<br/>Chromosome Duplication--genetics<br/>Chromosomes, Human, Pair 19--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence