Jones, Krystal M <br/><br/>
Adams-Oliver Syndrome Type 2 in Association with Compound Heterozygous DOCK6 Mutations.  [electronic resource] 

 -  Pediatric dermatology  Sep 2017 
 - e249-e253 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1525-1470 
<br/><br/><label>Standard No.: </label>10.1111/pde.13239  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ectodermal Dysplasia--diagnosis<br/>Guanine Nucleotide Exchange Factors--genetics<br/>Heterozygote<br/>Humans<br/>Infant, Newborn<br/>Limb Deformities, Congenital--diagnosis<br/>Magnetic Resonance Imaging<br/>Male<br/>Mutation<br/>Scalp Dermatoses--congenital