Stockton, D W <br/><br/>
Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.  [electronic resource] 

 -  American journal of medical genetics  Aug 1997 
 - 189-93 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0148-7299 
<br/><br/><label>Standard No.: </label>10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Banding<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 1--genetics<br/>Craniofacial Abnormalities--genetics<br/>Female<br/>Hand Deformities, Congenital--genetics<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Phenotype