Publication Name	World Journal of Medical Genetics
Manuscript ID	2119
Country	Iran

Received	2013-01-29 14:06
Peer-Review Started	2013-01-30 16:54
To Make the First Decision	2013-03-04 13:57
Return for Revision	2013-03-08 11:04
Revised	2013-03-11 14:56
Second Decision	2013-05-09 14:14
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief	2013-05-10 07:04
Articles in Press
Publication Fee Transferred
Edit the Manuscript by Language Editor	2013-05-30 04:19
Typeset the Manuscript	2013-06-09 20:09
Publish the Manuscript Online	2013-07-19 16:11

ISSN	2220-3184 (online)
Open Access
Copyright
Article Reprints	For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
Permissions	For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
Publisher	Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
Website	http://www.wjgnet.com

Category	Medicine, General & Internal
Manuscript Type	Autobiography
Article Title	Malignant pheochromocytoma in neurofibromatosis; mutation screening of RET proto-oncogene, VHL and SDH gene
Manuscript Source	Invited Manuscript
All Author List	Shirin Hasani-Ranjbar, Mahsa M Amoli, Maasumeh Noorani and Mohsen Ghadami
Funding Agency and Grant Number
Corresponding Author	Shirin Hasani-Ranjbar, Endocrinologist, Obesity and Eating Habits Research Center, Endocrinology and Metabolism Cellular and Molecular Sciences Institute, Shariati Hospital, Tehran University of Medical Sciences, North Kargar Ave., Tehran 14114, Iran. sh_hasani@sina.tums.ac.ir
Key Words	Neurofibromatosis; Familial pheochromocytoma; Malignant pheochromocytoma; Metastatic pheochromocytoma; RET proto-oncogene; von Hippel-Lindau; Succinate dehydrogenase complex subunits
Core Tip	Malignant pheochromocytoma associated with neurofibromatosis (NF) is very rare. We screened for all possible mutations related to pheochromocytoma in a patient with NF and malignant pheochromocytoma but found no mutations. This negative result shows that the NF1 gene is responsible for this rare presentation.
Publish Date	2013-07-19 16:11
Citation	Hasani-Ranjbar S, Amoli MM, Noorani M, Ghadami M. Malignant pheochromocytoma in neurofibromatosis; mutation screening of RET proto-oncogene, VHL and SDH gene. World J Med Genet 2013; 3(1): 1-4
URL	http://www.wjgnet.com/2220-3184/full/v3/i1/1.htm
DOI	http://dx.doi.org/10.5496/wjmg.v3.i1.1

Full Article (PDF)	WJMG-3-1.pdf
Manuscript File	2119-Review.doc
Answering Reviewers	2119-Answering reviewers.docx
Copyright License Agreement	2119-Copyright assignment.pdf
Peer-review Report	2119-Peer review(s).pdf
Scientific Editor Work List	2119-Scientific editor work list.doc