B. Turkgenc Et Al. , "A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes," 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , vol.27, Gothenburg, Sweden, pp.1271, 2019
Turkgenc, B. Et Al. 2019. A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes. 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , (Gothenburg, Sweden), 1271.
Turkgenc, B., Aguilar, R. P., Curral, B., Lowther, C., Wilch, E. S., Talkowski, M., ... Morton, C.(2019). A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes . 52nd Conference of the European-Society-of-Human-Genetics (ESHG) (pp.1271). Gothenburg, Sweden
Turkgenc, B. Et Al. "A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes," 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, Sweden, 2019
Turkgenc, B. Et Al. "A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, pp.1271, 2019
Turkgenc, B. Et Al. (2019) . "A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes." 52nd Conference of the European-Society-of-Human-Genetics (ESHG) , Gothenburg, Sweden, p.1271.
@conferencepaper{conferencepaper, author={B. Turkgenc Et Al. }, title={A balanced translocation t(2;7)(p21;p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes}, congress name={52nd Conference of the European-Society-of-Human-Genetics (ESHG)}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1271} }