Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18

por Bagherizadeh, Eiman, Behjati, Farkhondeh, Saberi, Seyed Hoseinali, Shafeghati, Yousef
Publicado 2011

Fanconi-Bickel syndrome versus osteogenesis imperfeeta: An Iranian case with a novel mutation in glucose transporter 2 gene, and review of literature

por Hadipour, Fatemeh, Sarkheil, Peymaneh, Noruzinia, Mehrdad, Hadipour, Zahra, Baghdadi, Taghi, Shafeghati, Yousef
Publicado 2013

Evaluation of Methylation Status in the 5'UTR Promoter Region of the DBC2 Gene as a Biomarker in Sporadic Breast Cancer

por Hajikhan Mirzaei, Mehri, Noruzinia, Mehrdad, Karbassian, Hamid, Shafeghati, Yousef, Keyhanee, Mousa, Bidmeshki-Pour, Ali
Publicado 2012

Introducing a Quantitative Method to Calculate the Rate of Primary Infertility

por Akhondi, MM, Kamali, K, Ranjbar, F, Shafeghati, S, Ardakani, Z Behjati, Shirzad, M, Eslamifar, M, Mohammad, K, Parsaeian, M
Publicado 2012

Prevalence of Primary Infertility in Iran in 2010

por AKHONDI, Mohammad Mehdi, KAMALI, Koorosh, RANJBAR, Fahimeh, SHIRZAD, Mahdi, SHAFEGHATI, Shiva, BEHJATI ARDAKANI, Zohreh, GOODJANI, Abolfazl, PARSAEIAN, Mahboubeh, MOHAMMAD, Kazem
Publicado 2013

Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

por Colombo, Elisa Adele, Mutlu-Albayrak, Hatice, Shafeghati, Yousef, Balasar, Mine, Piard, Juliette, Gentilini, Davide, Di Blasio, Anna Maria, Gervasini, Cristina, Van Maldergem, Lionel, Larizza, Lidia
Publicado 2019

Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies

por Mohammadzadeh, Akbar, Akbaroghli, Susan, Aghaei-Moghadam, Ehsan, Mahdieh, Nejat, Badv, Reza Shervin, Jamali, Payman, Kariminejad, Roxana, Chavoshzadeh, Zahra, Ghasemi Firouzabadi, Saghar, Mansour Ghanaie, Roxana, Nozari, Ahoura, Banihashemi, Sussan, Hadipour, Fatemeh, Hadipour, Zahra, Kariminejad, Ariana, Najmabadi, Hossein, Shafeghati, Yousef, Behjati, Farkhondeh
Publicado 2019

Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic M...

por Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Sajedi, Firoozeh, Kahrizi, Kimia, Najafi, Mostafa, Ebrahimizade Ghasemlou, Behruz, Shafeghati, Yousef, Behnia, Fatemeh, Mohammadi Arya, Ali Reza, Karimi, Hossein, Hadipour, Fatemeh, Hadipour, Zahra, Jamali, Peyman, Kariminejad, Roxana, Darvish, Hossein, Bahman, Ideh, Bagherizadeh, Eiman, Najmabadi, Hossein, Vameghi, Roshanak
Publicado 2013