Name: PubCaseFinder
License: http://creativecommons.org/licenses/by/2.1/jp/
Keywords: PubCaseFinder,PCF,Rare Disease,Phenotype,Gene,Match,Assist

17q11.2 microduplication syndrome

17q11.2 microduplication syndrome is characterized by dysmorphic features and intellectual deficit.

Sparse eyelashes

Decreased density/number of eyelashes.

Total: 0

(per page)

PMID (PMCID)