Keleş, Z. Et Al. 2019. A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features. 13. Balkan Congress of Human Genetics , (Edirne, Turkey), 41.

Keleş, Z., Özyavuz Çubuk, P., Koç, A., & Erçal, M. D., (2019). A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features . 13. Balkan Congress of Human Genetics (pp.41). Edirne, Turkey

Keleş, ZÜLAL Et Al. "A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features," 13. Balkan Congress of Human Genetics, Edirne, Turkey, 2019

Keleş, ZÜLAL Et Al. "A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features." 13. Balkan Congress of Human Genetics , Edirne, Turkey, pp.41, 2019

Keleş, Z. Et Al. (2019) . "A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features." 13. Balkan Congress of Human Genetics , Edirne, Turkey, p.41.

@conferencepaper{conferencepaper, author={ZÜLAL KELEŞ Et Al. }, title={A de novo 6q21q22.33 deletion in a boy with microcephaly, developmental delay and dysmorphic features}, congress name={13. Balkan Congress of Human Genetics}, city={Edirne}, country={Turkey}, year={2019}, pages={41} }