A. D. Cakir Et Al. , "Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2, pp.179-182, 2018
Cakir, A. D. Et Al. 2018. Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2 , 179-182.
Cakir, A. D., Turan, H., AYKUT, A., DURMAZ, A., Ercan, O., & Evliyaoglu, O., (2018). Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation. JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2, 179-182.
Cakir, Aydilek Et Al. "Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation," JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2, 179-182, 2018
Cakir, Aydilek D. Et Al. "Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2, pp.179-182, 2018
Cakir, A. D. Et Al. (2018) . "Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation." JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.2, pp.179-182.
@article{article, author={Aydilek Dagdeviren Cakir Et Al. }, title={Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation}, journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY}, year=2018, pages={179-182} }