Parry, D M <br/><br/>
SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanoma.  [electronic resource] 

 -  American journal of medical genetics  Aug 1986 
 - 653-72 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/ajmg.1320240410  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aneuploidy<br/>Centromere--ultrastructure<br/>Chromosomes--ultrastructure<br/>Cranial Nerve Diseases--genetics<br/>Ectromelia--complications<br/>Female<br/>Growth Disorders--complications<br/>Heterochromatin--ultrastructure<br/>Humans<br/>Lymphocytes--ultrastructure<br/>Melanoma--complications<br/>Mitosis<br/>Paralysis--genetics<br/>Skin Neoplasms--complications<br/>Syndrome