Kardon, N B <br/><br/>
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?  [electronic resource] 

 -  American journal of medical genetics. Supplement  1986 
 - 239-45 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1040-3787 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.1320250627  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ectromelia--classification<br/>Femur--abnormalities<br/>Fibula--abnormalities<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Radiography<br/>Syndrome<br/>Ulna--abnormalities