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 | AVESİS

Çukurova Üniversitesi Akademik Veri Yönetim Sistemi

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

Atıf İçin Kopyala

Ender K., PEHLİVAN D., Tamar H., BAYRAM Y., Tomasz G., Claudia G., ...Daha Fazla

Genomic disorders 2014, 5 - 07 Mart 2014

Yayın Türü: Bildiri
Çukurova Üniversitesi Adresli: Hayır