HIZ, A. S. Et Al. 2014. MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY. 11th European Congress on Epileptology , (Stockholm, Sweden), 79.

HIZ, A. S., Agilkaya, S., Bayram, E., & CİNGÖZ, S., (2014). MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY . 11th European Congress on Epileptology (pp.79). Stockholm, Sweden

HIZ, AYŞE Et Al. "MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY," 11th European Congress on Epileptology, Stockholm, Sweden, 2014

HIZ, AYŞE S. Et Al. "MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY." 11th European Congress on Epileptology , Stockholm, Sweden, pp.79, 2014

HIZ, A. S. Et Al. (2014) . "MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY." 11th European Congress on Epileptology , Stockholm, Sweden, p.79.

@conferencepaper{conferencepaper, author={AYŞE SEMRA HIZ Et Al. }, title={MOLECULAR CHARACTERIZATION OF A FAMILIAL CHROMOSOME 9Q22.2-22.32 DELETION IN A PATIENT WITH CORPUS CALLOSUM AGENESIS AND INTRACTABLE EPILEPSY}, congress name={11th European Congress on Epileptology}, city={Stockholm}, country={Sweden}, year={2014}, pages={79} }