Yunis-Varón Syndrome: The First Report of Two Iranian Cases by Zahra Hadipour, Yousef Shafeghati, Fatemeh Hadipour

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A new methodology in generating Digital Plants in AVEVA PDMS from Navisworks® model by Reyhaneh Nasirifar, Shahram Shafeghati, Iman Valipour

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Progeroid Syndrome and Mutation in LMNA Gene: Report of Two Cases from Iran by Y Shafeghati, N Levy, G.M Martin

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Fraccaro Syndrome: Report of Two Iranian Cases: An Infant and an Adult in A Family by Fatemeh Hadipour, Yousef Shafeghati, Eiman Bagherizadeh, Farkhondeh Behjati, Zahra Hadipour

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Evaluation of Methylation Status in the 5'UTR Promoter Region of the DBC2 Gene as a Biomarker in Sporadic Breast Cancer by Ali Bidmeshki-Pour, Mousa Keyhanee, Yousef Shafeghati, Hamid Karbassian, Mehrdad Noruzinia, Mehri Hajikhan Mirzaei

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Cytogenetic analysis of 1284 cases of Down syndrome by M.H Kariminejhad, R Kariminejhad, F Azimi, N Nabavi nia, K Alavi, M.T Takyar, Y Shafeghati

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Introducing a Quantitative Method to Calculate the Rate of Primary Infertility by MM Akhondi, K Kamali, F Ranjbar, S Shafeghati, Z Behjati Ardakani, M Shirzad, M Eslamifar, K Mohammad, M Parsaeian

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Clinical heterogeneity and chromosome breakage in Iranian patients suspicious of Fanconi anemia by Ghasemi Firoozabadi S, Shafeghati Y, Keyhani E, Kariminejad R, Oloomi Z, Moosavi F, Amini F, Najmabadi H, Behiati F

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Connecxin 26 Gene Mutations in Non-Syndromic Hearing Loss in Hamadan Province by Yousef Shafeghati, Ahmad Ebrahimi, Marzieh Mohseni, Farzaneh Ostadi, Halleh Habibi, Hamid Poujafari, R.J.H Esmith, Hosein Najmabadi

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Prevalence of Primary Infertility in Iran in 2010. by Mohammad Mehdi Akhondi, Koorosh Kamali, Fahimeh Ranjbar, Mahdi Shirzad, Shiva Shafeghati, Zohreh Behjati Ardakani, Abolfazl Goodjani, Mahboubeh Parsaeian, Kazem Mohammad

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Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics by Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi

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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations by Elisa Adele Colombo, Hatice Mutlu-Albayrak, Yousef Shafeghati, Mine Balasar, Juliette Piard, Davide Gentilini, Davide Gentilini, Anna Maria Di Blasio, Cristina Gervasini, Lionel Van Maldergem, Lidia Larizza

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Investigation of Chromosomal Abnormalities and Microdeletion/Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies by Akbar Mohammadzadeh, Susan Akbaroghli, Ehsan Aghaei-Moghadam, Nejat Mahdieh, Reza Shervin Badv, Payman Jamali, Roxana Kariminejad, Zahra Chavoshzadeh, Saghar Ghasemi Firouzabadi, Roxana Mansour Ghanaie, Ahoura Nozari, Sussan Banihashemi, Fatemeh Hadipour, Zahra Hadipour, Ariana Kariminejad, Hossein Najmabadi, Yousef Shafeghati, Farkhondeh Behjati

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