EKİNCİ, F. Et Al. 2020. A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.6 .

EKİNCİ, F., YILDIZDAŞ, R. D., ÖZGÜR HOROZ, Ö., Herguner, O., & BİŞGİN, A., (2020). A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction. EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.6.

EKİNCİ, FARUK Et Al. "A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction," EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.6, 2020

EKİNCİ, FARUK Et Al. "A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.6, 2020

EKİNCİ, F. Et Al. (2020) . "A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction." EUROPEAN JOURNAL OF MEDICAL GENETICS , vol.63, no.6.

@article{article, author={FARUK EKİNCİ Et Al. }, title={A homozygote frameshift mutation in OCLN gene result in Pseudo-TORCH syndrome type I: A case report extending the phenotype with central diabetes insipidus and renal dysfunction}, journal={EUROPEAN JOURNAL OF MEDICAL GENETICS}, year=2020}