TY - JOUR T1 - Autosomal dominant asymmetrical radial dysplasia, dysmorphic facies, and conductive hearing loss (facioauriculoradial dysplasia) JF - Journal of Medical Genetics JO - J Med Genet SP - 110 LP - 115 DO - 10.1136/jmg.19.2.110 VL - 19 IS - 2 AU - A E Harding AU - C M Hall AU - M Baraitser Y1 - 1982/04/01 UR - http://jmg.bmj.com/content/19/2/110.abstract N2 - A syndrome characterised by asymmetrical radial dysplasia, dysmorphic facies, conductive deafness, and external ear deformity is described in a mother and her daughter. This combination of anomalies has previously been reported in members of a single family. The disorder appears to be clinically and genetically distinct from others associated with radial dysplasia, such as Nager's acrofacial dysostosis and the lachrimoauriculoradiodental syndrome. Inheritance is autosomal dominant, with marked variation in expression of the mutant gene. ER -