Kantarci, S <br/><br/>
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jan 2006 
 - 17-23 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31025  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1--genetics<br/>Cleft Palate--pathology<br/>Craniofacial Abnormalities--pathology<br/>Fatal Outcome<br/>Genetic Predisposition to Disease--genetics<br/>Genome, Human<br/>Hernia, Diaphragmatic--genetics<br/>Hernias, Diaphragmatic, Congenital<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Infant, Newborn<br/>Karyotyping<br/>Limb Deformities, Congenital--pathology<br/>Nails, Malformed<br/>Nucleic Acid Hybridization--methods<br/>Syndrome