Tekguc, D. C. Et Al. 2022. Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1 , 255.

Tekguc, D. C., Tuncel, G., Karanlik, S., Koreken, N., TEMEL, Ş. G., & Ergoren, M. C., (2022). Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly. EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 255.

Tekguc, Doga Et Al. "Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly," EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, 255, 2022

Tekguc, Doga C. Et Al. "Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, pp.255, 2022

Tekguc, D. C. Et Al. (2022) . "Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly." EUROPEAN JOURNAL OF HUMAN GENETICS , vol.30, no.SUPPL 1, p.255.

@article{article, author={Doga Ceren Tekguc Et Al. }, title={Characterizing a de novo TRIO gene variant as a likely cause of autosomal dominant Intellectual developmental disorder type 63 with macrocephaly}, journal={EUROPEAN JOURNAL OF HUMAN GENETICS}, year=2022, pages={255} }