Feingold, M <br/><br/>
Case report. Case 1 (Conradi syndrome, autosomal dominant type).  [electronic resource] 

 -  Birth defects original article series  1974 
 - 93-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0547-6844 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chondrodysplasia Punctata--diagnostic imaging<br/>Chromosomes, Human, 21-22 and Y<br/>Diagnosis, Differential<br/>Face<br/>Genes, Dominant<br/>Humans<br/>Infant<br/>Karyotyping<br/>Male<br/>Radiography