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

Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome

Micrognathia

Developmental hypoplasia of the mandible.

Total: 0

(per page)

PMID (PMCID)