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
Published 2013-12-01

Combination of Genetics and Nanotechnology for Down Syndrome Modification: A Potential Hypothesis and Review of the Literature

by Alireza TAFAZOLI, Farkhondeh BEHJATI, Dariush D. FARHUD, Mohammad Reza ABBASZADEGAN
Published 2019-03-01

A Pathogenic Homozygous Mutation In The Pleckstrin Homology Domain Of RASA1 Is Responsible For Familial Tricuspid Atresia In An Iranian Consanguineous Family

by Ahoura Nozari, Ehsan Aghaei-Moghadam, Aliakbar Zeinaloo, Afagh Alavi, Saghar Ghasemi Firouzabad, Shohre Minaee, Marzeieh Eskandari Hesari, Farkhondeh Behjati
Published 2018-12-01

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

by Maryam Najafi, Dor Mohammad Kordi-Tamandani, Farkhondeh Behjati, Simin Sadeghi-Bojd, Zeineb Bakey, Ehsan Ghayoor Karimiani, Isabel Schüle, Anoush Azarfar, Miriam Schmidts
Published 2019-02-01

Accurate Breakpoint Mapping in Apparently Balanced Translocation Families with Discordant Phenotypes Using Whole Genome Mate-Pair Sequencing.

by Constantia Aristidou, Costas Koufaris, Athina Theodosiou, Mads Bak, Mana M Mehrjouy, Farkhondeh Behjati, George Tanteles, Violetta Christophidou-Anastasiadou, Niels Tommerup, Carolina Sismani
Published 2017-01-01

Genetic Causes of Mental Retardation in Golestan Province

by Hossein Darvish, Saghar Ghasemi-Firouzabadi, Gholam Reza Bahrami-Monajemi, Ideh Bahman, Marziyeh Mohseni, Mohammad Javad Soltani-Banavandi, Sousan Banihashemi , Sanaz Arjangi, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi
Published 2010-10-01

A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East

by Maryam Najafi, Maryam Najafi, Dor Mohammad Kordi Tamandani, Anoush Azarfar, Zeineb Bakey, Zeineb Bakey, Farkhondeh Behjati, Dinu Antony, Dinu Antony, Isabel Schüle, Simin Sadeghi-Bojd, Ehsan Ghayoor Karimiani, Ehsan Ghayoor Karimiani, Miriam Schmidts, Miriam Schmidts
Published 2019-03-01

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
Published 2019-06-01

BOD1 Is Required for Cognitive Function in Humans and Drosophila.

by Sahar Esmaeeli-Nieh, Michaela Fenckova, Iain M Porter, M Mahdi Motazacker, Bonnie Nijhof, Anna Castells-Nobau, Zoltan Asztalos, Robert Weißmann, Farkhondeh Behjati, Andreas Tzschach, Ute Felbor, Harry Scherthan, Seyed Morteza Sayfati, H Hilger Ropers, Kimia Kahrizi, Hossein Najmabadi, Jason R Swedlow, Annette Schenck, Andreas W Kuss
Published 2016-05-01