Melnick, M <br/><br/>
Dentin dysplasia, type II: a rare autosomal dominant disorder.  [electronic resource] 

 -  Oral surgery, oral medicine, and oral pathology  Oct 1977 
 - 592-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0030-4220 
<br/><br/><label>Standard No.: </label>10.1016/0030-4220(77)90303-6  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Chromosomes, Human<br/>Dentin--ultrastructure<br/>Dentin Dysplasia--genetics<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Male<br/>Pedigree