Boycott, Kym M <br/><br/>
A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2010 
 - 1349-56 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.33379  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adolescent<br/>Adult<br/>Child<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 16--genetics<br/>Developmental Disabilities--diagnosis<br/>Facies<br/>Female<br/>Genetic Markers<br/>Humans<br/>Pedigree<br/>Population--genetics<br/>Syndrome<br/>Young Adult