Sarı Tunel, F. Et Al. 2019. Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease. 13th Balkan Congress of Human Genetics , (Edirne, Turkey), 76.

Sarı Tunel, F., Tuncer Kılınç, F. N., Bayrak, A. E., Salman Yılmaz, S., Oflazer, P., & Vural, B., (2019). Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease . 13th Balkan Congress of Human Genetics (pp.76). Edirne, Turkey

Sarı Tunel, Fatma Et Al. "Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease," 13th Balkan Congress of Human Genetics, Edirne, Turkey, 2019

Sarı Tunel, Fatma S. Et Al. "Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease." 13th Balkan Congress of Human Genetics , Edirne, Turkey, pp.76, 2019

Sarı Tunel, F. Et Al. (2019) . "Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease." 13th Balkan Congress of Human Genetics , Edirne, Turkey, p.76.

@conferencepaper{conferencepaper, author={Fatma Sarı Tunel Et Al. }, title={Whole Exome Sequence Analyses In A Consanguıneous Famıly Wıth Affected Dizygotic Twins Reveal A Novel SEPN1 Variant Associated With Multiminicore Disease}, congress name={13th Balkan Congress of Human Genetics}, city={Edirne}, country={Turkey}, year={2019}, pages={76} }