Faria, Ágatha Cristhina <br/><br/>
Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2016 
 - 403-409 p.  digital 
<br/><br/> Publication Type: 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.37448  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Brain--abnormalities<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 10--genetics<br/>Comparative Genomic Hybridization<br/>Craniosynostoses--etiology<br/>Facies<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Learning Disabilities--etiology<br/>Male<br/>Prognosis<br/>Sutures--adverse effects