M. Ç. ERGÖREN Et Al. , "High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.," 13.Balkan Congress Of Human Genetics , 2019
ERGÖREN, M. Ç. Et Al. 2019. High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.. 13.Balkan Congress Of Human Genetics .
ERGÖREN, M. Ç., AKCAN, N., YÜKSEL, Ü., ÖZEMRİ SAĞ, Ş., & TEMEL, Ş. G., (2019). High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient. . 13.Balkan Congress Of Human Genetics
ERGÖREN, MAHMUT Et Al. "High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.," 13.Balkan Congress Of Human Genetics, 2019
ERGÖREN, MAHMUT Ç. Et Al. "High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.." 13.Balkan Congress Of Human Genetics , 2019
ERGÖREN, M. Ç. Et Al. (2019) . "High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.." 13.Balkan Congress Of Human Genetics .
@conferencepaper{conferencepaper, author={MAHMUT ÇERKEZ ERGÖREN Et Al. }, title={High-throughput DNA sequencing-based genomic profiling analysis reveals novelhomozygote mutations-phenotype association for severe dilated cardiomyopathy in a Turkishheritage patient.}, congress name={13.Balkan Congress Of Human Genetics}, city={}, country={}, year={2019}}