Archer, H L <br/><br/>
Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jul 2005 
 - 38-44 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30774  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 19--genetics<br/>Cleft Palate--pathology<br/>Face--abnormalities<br/>Genetic Predisposition to Disease--genetics<br/>Hearing Loss--pathology<br/>Heart Defects, Congenital--pathology<br/>Humans<br/>Immune System--abnormalities<br/>In Situ Hybridization, Fluorescence<br/>Keloid--pathology<br/>Learning Disabilities--pathology<br/>Male<br/>Phenotype<br/>Telomere--genetics