Noriko Funato, Junko Nohtomi-Ohyama, Kimie Ohyama. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsCraniofacial DysostosisDiseases in Twins/geneticsFemaleHeart Septal Defects, VentricularHumansMutation, MissenseReceptor Protein-Tyrosine Kinases/geneticsReceptor, Fibroblast Growth Factor, Type 2Receptors, Fibroblast Growth Factor/geneticsSyndromeTwins, Monozygotic
Substances: See more » Receptors, Fibroblast Growth FactorFGFR2 protein, humanReceptor Protein-Tyrosine KinasesReceptor, Fibroblast Growth Factor, Type 2
Year: 2005 PMID: 15669095 DOI: 10.1002/ajmg.a.30581
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802