T Trummer, D Müller, A Schulze, W Vogel, W Just. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Abnormalities, Multiple/geneticsBranchio-Oto-Renal Syndrome/geneticsCleft Lip/geneticsCraniofacial Abnormalities/geneticsEye Abnormalities/geneticsFemaleHearing Loss, Sensorineural/geneticsHumansMalePedigreeSkin Abnormalities/geneticsSyndrome
Year: 2002 PMID： 11826031 PMCID： PMC1734969 DOI： 10.1136/jmg.39.1.71
Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318