F. E. Perçin Et Al. , "A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes," ERCIYES MEDICAL JOURNAL , vol.40, no.2, pp.69, 2018
Perçin, F. E. Et Al. 2018. A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes. ERCIYES MEDICAL JOURNAL , vol.40, no.2 , 69.
Perçin, F. E., Kayhan, G., Sezer, A., Koc, A., & Ergün, M. A., (2018). A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes. ERCIYES MEDICAL JOURNAL , vol.40, no.2, 69.
Perçin, FERDA Et Al. "A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes," ERCIYES MEDICAL JOURNAL , vol.40, no.2, 69, 2018
Perçin, FERDA E. Et Al. "A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes." ERCIYES MEDICAL JOURNAL , vol.40, no.2, pp.69, 2018
Perçin, F. E. Et Al. (2018) . "A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes." ERCIYES MEDICAL JOURNAL , vol.40, no.2, p.69.
@article{article, author={FERDA EMRİYE PERÇİN Et Al. }, title={A patıent wıth two syndromes due to paternal unıparental dısomy of chromosome 2 (pUPD2) related wıth homozygous novel mutatıons of the RAB3GAP1 and UNC80 genes}, journal={ERCIYES MEDICAL JOURNAL}, year=2018, pages={69} }