Ender, K. Et Al. 2014. Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations. Genomic disorders 2014 .

Ender, K., PEHLİVAN, D., Tamar, H., BAYRAM, Y., Tomasz, G., Claudia, G., ... Bo, Y.(2014). Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations . Genomic disorders 2014

Ender, Karaca Et Al. "Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations," Genomic disorders 2014, 2014

Ender, Karaca Et Al. "Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations." Genomic disorders 2014 , 2014

Ender, K. Et Al. (2014) . "Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations." Genomic disorders 2014 .

@conferencepaper{conferencepaper, author={Karaca Ender Et Al. }, title={Whole Exome Sequencing Identifies Rare Variants in Turkish Patients with Brain Malformation and Underscores the Power of Rare Variants Identified by Genomic Sequencing Approaches in Selected World Populations}, congress name={Genomic disorders 2014}, city={}, country={}, year={2014}}