Pebrel-Richard, Celine <br/><br/>
Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay.  [electronic resource] 

 -  American journal of medical genetics. Part A  Nov 2014 
 - 2964-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.36715  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Duplication<br/>Chromosomes, Human, Pair 7<br/>Comparative Genomic Hybridization<br/>Craniofacial Abnormalities--diagnosis<br/>Facies<br/>Humans<br/>Language Development Disorders--diagnosis<br/>Male<br/>Phenotype<br/>Syndrome