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.