D. KAYA Et Al. , "A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE," 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 , Skopje, Macedonia, 2023
KAYA, D. Et Al. 2023. A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE. 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 , (Skopje, Macedonia).
KAYA, D., AKCAN, M. B., CEYLAN KÖSE, C., & SILAN, F., (2023). A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE . 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Macedonia
KAYA, DERYA Et Al. "A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE," 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023, Skopje, Macedonia, 2023
KAYA, DERYA Et Al. "A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE." 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 , Skopje, Macedonia, 2023
KAYA, D. Et Al. (2023) . "A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE." 14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023 , Skopje, Macedonia.
@conferencepaper{conferencepaper, author={DERYA KAYA Et Al. }, title={A CASE REPORT OF A PATIENT WITH NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS: A NOVEL BIALLELIC VARIANT IN ZNF142 GENE}, congress name={14th Balkan Congress of Human Genetics & 9th Rare Disease SEE Meeting 2023}, city={Skopje}, country={Macedonia}, year={2023}}