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Search Results - Khakpour, Golnaz
Search Results - Khakpour, Golnaz
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Over expression of circulating miR-155 predicts prognosis in diffuse large B-cell lymphoma
by
Ahmadvand, Mohammad
,
Eskandari, Mahsa
,
Pashaiefar, Hossein
,
Yaghmaie, Marjan
,
Manoochehrabadi, Saba
,
Khakpour, Golnaz
,
Sheikhsaran, Fatemeh
,
Montazer Zohour, Mostafa
Published in
Leukemia research
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Methylomics of breast cancer: Seeking epimarkers in peripheral blood of young subjects
by
Khakpour, Golnaz
,
Noruzinia, Mehrdad
,
Izadi, Pantea
,
Karami, Fatemeh
,
Ahmadvand, Mohammad
,
Heshmat, Ramin
,
Amoli, Mahsa M
,
Tavakkoly-Bazzaz, Javad
Published in
Tumor biology
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A meta-analysis of different von Hippel Lindau mutations: are they related to retinal capillary hemangioblastoma?
by
Azimi, Fatemeh
,
Aghajani, Ali
,
Khakpour, Golnaz
,
Chaibakhsh, Samira
Published in
Molecular genetics and genomics : MGG
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Use of expanded carrier screening for retrospective diagnosis of two deceased siblings with Van Maldergem syndrome 2: case report
by
Rahmani, Nasim
,
Ahmadvand, Mohammad
,
Khakpour, Golnaz
Published in
Asian biomedicine
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Young Breast Cancer: Novel Gene Methylation in WBC
by
Noruzinia, Mehrdad
,
Tavakkoly-Bazzaz, Javad
,
Ahmadvand, Mohammad
,
Azimi, Fatemeh
,
Dehghanifard, Ali
,
Khakpour, Golnaz
Published in
Asian Pacific journal of cancer prevention : APJCP
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Investigation of germline VHL variants in Iranian patients with retinal capillary hemangioblastoma and genotype-phenotype analysis
by
Naseripour, Masood
,
Azimi, Fatemeh
,
Talebi, Said
,
Mirshahi, Reza
,
Kiaee, Reza
,
Sedaghat, Ahad
,
Zohre, Ataei Kachoei
,
Khakpour, Golnaz
Published in
Ophthalmic genetics
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Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion
by
Hemmati, Sara
,
Khakpour, Golnaz
,
Nadjafi-Semnani, Fatemeh
,
Gordiz, Arzhang
,
Sajadi, Masoome
,
Abdi, Fatemeh
Published in
Ophthalmic genetics
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DNA methylation as a promising landscape: A simple blood test for breast cancer prediction
by
Khakpour, Golnaz
,
Pooladi, Arash
,
Izadi, Pantea
,
Noruzinia, Mehrdad
,
Tavakkoly Bazzaz, Javad
Published in
Tumor biology
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Genetic Screening of Iranian Patients with 46,XY Disorders of Sex Development
by
Shojaei, Azadeh
,
Ebrahimzadeh-Vesal, Reza
,
Ahani, Ali
,
Razzaghy-Azar, Maryam
,
Khakpour, Golnaz
,
Ghazi, Farideh
,
Tavakkoly-Bazzaz, Javad
Published in
Reports of biochemistry and molecular biology
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Investigation of germline VHL variants in Iranian patients with retinal capillary hemangioblastoma and genotype-phenotype analysis
by
Naseripour, Masood
,
Azimi, Fatemeh
,
Talebi, Said
,
Mirshahi, Reza
,
Kiaee, Reza
,
Sedaghat, Ahad
,
Zohre, Ataei Kachoei
,
Khakpour, Golnaz
Published in
Ophthalmic Genetics
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Heterozygote MTHFR A1298C mutation in a case of autosomal recessive bestrophinopathy with branch retinal vein occlusion
by
Hemmati, Sara
,
Khakpour, Golnaz
,
Nadjafi-Semnani, Fatemeh
,
Gordiz, Arzhang
,
Sajadi, Masoome
,
Abdi, Fatemeh
Published in
Ophthalmic genetics
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