Fernandez, Thomas V <br/><br/>
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.  [electronic resource] 

 -  American journal of medical genetics. Part A  Nov 2008 
 - 2746-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32533  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 13--genetics<br/>Chromosomes, Human, Pair 3--genetics<br/>Comparative Genomic Hybridization<br/>Craniofacial Abnormalities--genetics<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Limb Deformities, Congenital--genetics<br/>Male<br/>Phenotype<br/>Syndrome<br/>Translocation, Genetic