Citation Analysis of Papers of Research Projects at Faculty of Dentistry, Tabriz University of Medical Sciences

por Esmaeilzadeh Hojbi, Sima, Ghaffari, Saeed
Publicado 2011

Investigation of QF-PCR Application for Rapid Prenatal Diagnosis of Chromosomal Aneuploidies in Iranian Population

por Nasiri, Habib, Noori-Dalooi, Mohammad-Reza, Dastan, Jila, Ghaffari, Saeed-Reza
Publicado 2011

Non-progressive Nonimmune Hydrops Fetalis Caused by a Novel Mutation in GUSB Gene

por MOSALLANEJAD, Asieh, ALAEI, Mohammadreza, GHAFFARI, Saeed Reza, RAFATI, Maryam, SANEIFARD, Hedyeh
Publicado 2020

Paradox of Modern Pregnancy: A Phenomenological Study of Women's Lived Experiences from Assisted Pregnancy

por Ranjbar, Fahimeh, Akhondi, Mohammad-Mehdi, Borimnejad, Leili, Ghaffari, Saeed-Reza, Behboodi-Moghadam, Zahra
Publicado 2015

Experiences of Infertile Women Seeking Assisted Pregnancy in Iran: A Qualitative Study

por Ranjbar, Fahimeh, Behboodi-Moghadam, Zahra, Borimnejad, Leili, Ghaffari, Saeed Reza, Akhondi, Mohammad Mehdi
Publicado 2015

Detection of Aneuploidies in Products of Conception and Neonatal Deaths in Iranian Patients Using the Multiplex Ligation-Dependent Probe Amplification (MLPA)

por Khorami Sarvestani, Sara, Rafati, Maryam, Soltanghoraee, Haleh, Hoseini, Azadeh, Soltani, Azadeh, Jalilian, Koosha, Ghaffari, Saeed Reza
Publicado 2021

"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements

por Rafati, Maryam, Ghadirzadeh, Mohammad R, Heshmati, Yaser, Adibi, Homeira, Keihanidoust, Zarrintaj, Eshraghian, Mohammad R, Dastan, Jila, Hoseini, Azadeh, Purhoseini, Marzieh, Ghaffari, Saeed R
Publicado 2012

"Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromes

por Rafati, Maryam, Seyyedaboutorabi, Elaheh, Ghadirzadeh, Mohammad R, Heshmati, Yaser, Adibi, Homeira, Keihanidoust, Zarrintaj, Eshraghian, Mohammad R, Javadi, Gholam Reza, Dastan, Jila, Mosavi-Jarrahi, Alireza, Hoseini, Azadeh, Purhoseini, Marzieh, Ghaffari, Saeed R
Publicado 2012

Increasing the Yield in Targeted Next-Generation Sequencing by Implicating CNV Analysis, Non-Coding Exons and the Overall Variant Load: The Example of Retinal Dystrophies

por Eisenberger, Tobias, Neuhaus, Christine, Khan, Arif O., Decker, Christian, Preising, Markus N., Friedburg, Christoph, Bieg, Anika, Gliem, Martin, Issa, Peter Charbel, Holz, Frank G., Baig, Shahid M., Hellenbroich, Yorck, Galvez, Alberto, Platzer, Konrad, Wollnik, Bernd, Laddach, Nadja, Ghaffari, Saeed Reza, Rafati, Maryam, Botzenhart, Elke, Tinschert, Sigrid, Börger, Doris, Bohring, Axel, Schreml, Julia, Körtge-Jung, Stefani, Schell-Apacik, Chayim, Bakur, Khadijah, Al-Aama, Jumana Y., Neuhann, Teresa, Herkenrath, Peter, Nürnberg, Gudrun, Nürnberg, Peter, Davis, John S., Gal, Andreas, Bergmann, Carsten, Lorenz, Birgit, Bolz, Hanno J.
Publicado 2013