Phenotypical characterization of 13q deletion syndrome: Report of two cases

por Bagherizadeh, Eiman, Shafaghati, Yousef, Hadipour, Fatemeh, Behjati, Farkhondeh
Publicado 2014

Evaluation of chromosomal aberrations caused by air pollutants in some taxi drivers from two polluted districts of urban Tehran and its comparison with drivers from rural areas of...

por Taghizadeh, Sara, Najmabadi, Hossein, Kamali, Koorosh, Behjati, Farkhondeh
Publicado 2014

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

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

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

por TAFAZOLI, Alireza, BEHJATI, Farkhondeh, FARHUD, Dariush D., ABBASZADEGAN, Mohammad Reza
Publicado 2019

The Genotoxic and Cytotoxic Effects of Bisphenol-A (BPA) in MCF-7 Cell Line and Amniocytes

por Aghajanpour-Mir, Seyed Mohsen, Zabihi, Ebrahim, Akhavan-Niaki, Haleh, Keyhani, Elahe, Bagherizadeh, Iman, Biglari, Sajjad, Behjati, Farkhondeh
Publicado 2016

A Pathogenic Homozygous Mutation in The Pleckstrin Homology Domain of RASA1 Is Responsible for Familial Tricuspid Atresia in An Iranian Consanguineous Family

por Nozari, Ahoura, Aghaei-Moghadam, Ehsan, Zeinaloo, Aliakbar, Alavi, Afagh, Ghasemi Firouzabdi, Saghar, Minaee, Shohre, Eskandari Hesari, Marzieh, Behjati, Farkhondeh
Publicado 2019

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

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

Relationship Between PIK3CA Amplification and P110α and CD34 Tissue Expression as Angiogenesis Markers in Iranian Women with Sporadic Breast Cancer

por Hosseini, Shadi, Behjati, Farkhondeh, Rahimi, Maryam, Taheri, Nazanin, Khoram Khorshid, Hamidreza, Aghakhani Moghaddam, Fatemeh, Ghasemi, Saghar, Karimlou, Masoud, Sirati, Fereidoon, Keyhani, Elahe
Publicado 2018

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

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

Mutation Screening of BRCA Genes in 10 Iranian Males with Breast Cancer

por Zorrieh Zahra, Atieh, Kadkhoda, Sepideh, Behjati, Farkhondeh, Aghakhani Moghaddam, Fatemeh, Badiei, Azadeh, Sirati, Fereidoon, Afshin Alavi, Hossein, Atri, Morteza, Omranipour, Ramesh, Keyhani, Elahe
Publicado 2016

Exploring the Genetic Causality of Discordant Phenotypes in Familial Apparently Balanced Translocation Cases Using Whole Exome Sequencing

por Aristidou, Constantia, Theodosiou, Athina, Alexandrou, Angelos, Papaevripidou, Ioannis, Evangelidou, Paola, Kosmaidou-Aravidou, Zoe, Behjati, Farkhondeh, Christophidou-Anastasiadou, Violetta, Tanteles, George A., Sismani, Carolina
Publicado 2022

Genomic characterization of some Iranian children with idiopathic mental retardation using array comparative genomic hybridization

por Behjati, Farkhondeh, Firouzabadi, Saghar Ghasemi, Kariminejad, Roxana, Vameghi, Roshanak, Sajedi, Firouzeh, Shafaghati, Yousef, Ghasemlou, Behruz Ebrahimizade, Shojaei, Azadeh, Jamali, Peyman, Bahman, Ideh, Najmabadi, Hossein
Publicado 2013

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

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

Chromosome abnormality rate among Iranian patients with idiopathic mental retardation from consanguineous marriages

por Behjati, Farkhondeh, Ghasemi Firouzabadi, Saghar, Kahrizi, Kimia, Kariminejad, Roxana, Bagherizadeh, Iman, Ansari, Javad, Fallah, Masoumeh, Mojtahedi, Forough, Darvish, Hossein, Bahrami Monajemi, Gholamreza, Abedini, S. Sedigheh, Jamali, Payman, Mojahedi, Faezeh, Zadeh-Vakili, Azita, Najmabadi, Hossein
Publicado 2011

Analysis of Copy Number Variations in Patients with Autism Using Cytogenetic and MLPA Techniques: Report of 16p13.1p13.3 and 10q26.3 Duplications

por Ghasemi Firouzabadi, Saghar, Vameghi, Roshanak, Kariminejad, Roxana, Darvish, Hossein, Banihashemi, Susan, Firouzkouhi Moghaddam, Mahboubeh, Jamali, Peyman, Farbod Mofidi Tehrani, Hassan, Dehghani, Hossein, Raeisoon, Mohammad Reza, Narooie-Nejad, Mehrnaz, Jamshidi, Javad, Tafakhori, Abbas, Sadabadi, Saeid, Behjati, Farkhondeh
Publicado 2016

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

BOD1 Is Required for Cognitive Function in Humans and Drosophila

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