2018
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. and Reutter, H. and Marsch, F. and Thiele, H. and Altmüller, J. and Ludwig, M. and Zhang, R.
Molecular Medicine Reports 17
(2): 3200-3205.
February 2018
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