Condition: Atresia of the external auditory canal


rs864309486 in GMNN gene and Atresia of the external auditory canal PMID 26637980 2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.

rs793888541 in TFAP2A-AS2;TFAP2A gene and Atresia of the external auditory canal PMID 25590586 2015 A clinical and molecular analysis of branchio-oculo-facial syndrome patients in Russia revealed new mutations in TFAP2A.