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

2p15p16.1 microdeletion syndrome

2p15p16.1 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.

Retrognathia

An abnormality in which the mandible is mislocalised posteriorly.

合計: 0

（表示件数）

PMID (PMCID)