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Whole exome sequencing identifies a mutation in EYA1 and GLI3 in a patient with branchio‑otic syndrome and esophageal atresia: Coincidence or a digenic mode of inheritance?
Kause, F., Reutter, H., Marsch, F., Thiele, H., Altmüller, J. 
ORCID: https://orcid.org/0000-0003-4372-1521, Ludwig, M. and Zhang, R.
Molecular Medicine Reports 17
(2): 3200-3205.
February 2018
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