H. Cangul Et Al. , "Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism," 50th European-Society-of-Human-Genetics (ESHG) Conference , vol.26, Copenhagen, Denmark, pp.198, 2017
Cangul, H. Et Al. 2017. Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism. 50th European-Society-of-Human-Genetics (ESHG) Conference , (Copenhagen, Denmark), 198.
Cangul, H., Ozel, M., Genc, N., Kardelen, A. D., & Darendeliler, F., (2017). Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism . 50th European-Society-of-Human-Genetics (ESHG) Conference (pp.198). Copenhagen, Denmark
Cangul, H. Et Al. "Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism," 50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, Denmark, 2017
Cangul, H. Et Al. "Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, pp.198, 2017
Cangul, H. Et Al. (2017) . "Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism." 50th European-Society-of-Human-Genetics (ESHG) Conference , Copenhagen, Denmark, p.198.
@conferencepaper{conferencepaper, author={H. Cangul Et Al. }, title={Development of the most comprehensive genetic test based on next generation sequencing for diagnosis of congenital hypothyroidism}, congress name={50th European-Society-of-Human-Genetics (ESHG) Conference}, city={Copenhagen}, country={Denmark}, year={2017}, pages={198} }