Turkgenc, B. And TEMEL, Ş. G. 2019. A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes. EUROPEAN JOURNAL OF HUMAN GENETICS , (Gothenburg, Sweden), 1271.

Turkgenc, B., & TEMEL, Ş. G., (2019). A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes . EUROPEAN JOURNAL OF HUMAN GENETICS (pp.1271). Gothenburg, Sweden

Turkgenc, Burcu, And ŞEHİME GÜLSÜN TEMEL. "A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes," EUROPEAN JOURNAL OF HUMAN GENETICS, Gothenburg, Sweden, 2019

Turkgenc, Burcu And TEMEL, ŞEHİME G. . "A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes." EUROPEAN JOURNAL OF HUMAN GENETICS , Gothenburg, Sweden, pp.1271, 2019

Turkgenc, B. And TEMEL, Ş. G. (2019) . "A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes." EUROPEAN JOURNAL OF HUMAN GENETICS , Gothenburg, Sweden, p.1271.

@conferencepaper{conferencepaper, author={Burcu Turkgenc And author={ŞEHİME GÜLSÜN TEMEL}, title={A balanced translocation t(27)(p21p15) in three generations: Genome sequencing offers an opportunity to understand molecular etiology of Saethre-Chotzen/Robinow-Sarouf syndromes}, congress name={EUROPEAN JOURNAL OF HUMAN GENETICS}, city={Gothenburg}, country={Sweden}, year={2019}, pages={1271} }