PgmNr 2987: The utility of a next generation sequencing panel in severe pediatric onset inherited diseases.


IŞIK E. , ONAY H. , ATİK T. , Canda E. , ÇOĞULU M. Ö. , ÖZKINAY F. F.

AMERICAN SOCIETY OF HUMAN GENETICS ANNUAL MEETING - SAN DIEGO, 16 - 21 Ekim 2018