Grønborg, Sabine <br/><br/>
Monozygotic twins with a de novo 0.32 Mb 16q24.3 deletion, including TUBB3 presenting with developmental delay and mild facial dysmorphism but without overt brain malformation.  [electronic resource] 

 -  American journal of medical genetics. Part A  Nov 2015 
 - 2731-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Twin Study 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.37227  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Pairing--genetics<br/>Brain--abnormalities<br/>Chromosomes, Human, Pair 16--genetics<br/>Comparative Genomic Hybridization<br/>Developmental Disabilities--genetics<br/>Facies<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Magnetic Resonance Imaging<br/>Sequence Deletion<br/>Tubulin--genetics<br/>Twins, Monozygotic--genetics