Jehee, F S <br/><br/>
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly.  [electronic resource] 

 -  Clinical genetics  Jun 2005 
 - 503-10 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2005.00438.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 11<br/>Chromosomes, Human, Pair 9<br/>Cohort Studies<br/>Craniosynostoses--diagnosis<br/>Female<br/>Genetic Testing--methods<br/>Humans<br/>Infant<br/>Karyotyping<br/>Male<br/>Pedigree<br/>Phenotype