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Paper Details

A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.
Am J Hum Genet
64
2012
ACS, Auriculocondylar syndrome, DLX5, DLX5/6, DLX6, EDN1, GNAI3, PLCB4, PLCB4 mutations, amino-acid, autosomal-dominant craniofacial malformation syndrome, chromosomes, cleft palate, conserved, cultured osteoblasts, distal-less homeobox 5 and 6, ear malformation, endothelin-1, homeotic, human, humans, micrognathia, osteoblasts, patient, temporomandibular joint ankylosis
Author NameAffiliation
Mark J RiederUniversity of Washington
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Release 1.2