New translocation in acute myeloid leukemia M4 eos

ανά Bahoush, Gholamreza, Vafapour, Maryam, Kariminejad, Roxana
Τόπος έκδοσης Leuk Res Rep (2020)

Detection of New Translocation in Infant Twins with Concordant ALL and Discordant Outcome

ανά Bahoush, Golamreza, Vafapour, Maryam, Kariminejad, Roxana
Τόπος έκδοσης Pediatr Rep (2020)

Frequency of Sperm Aneuploidy in Oligoasthenoteratozoospermic (OAT) Patients by Comprehensive Chromosome Screening: A Proof of Concept

ανά Saei, Parishad, Bazrgar, Masood, Gourabi, Hamid, Kariminejad, Roxana, Eftekhari-Yazdi, Poopak, Fakhri, Mostafa
Τόπος έκδοσης J Reprod Infertil (2021)

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

ανά Najafi, Kimia, Mehrjoo, Zohreh, Ardalani, Fariba, Ghaderi-Sohi, Siavash, Kariminejad, Ariana, Kariminejad, Roxana, Najmabadi, Hossein
Τόπος έκδοσης Sci Rep (2021)

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

ανά Taghdiri, Maryam, Kashef, Atie, Abbassi, Golemaryam, Moshtagh, Azadeh, Sadatian, Neda, Fardaei, Majid, Najafi, Kimia, Kariminejad, Roxana
Τόπος έκδοσης Clin Case Rep (2019)

An autosomal recessive syndrome of severe mental retardation, cataract, coloboma and kyphosis maps to the pericentromeric region of chromosome 4

ανά Kahrizi, Kimia, Najmabadi, Hossein, Kariminejad, Roxana, Jamali, Payman, Malekpour, Mahdi, Garshasbi, Masoud, Ropers, Hans Hilger, Kuss, Andreas Walter, Tzschach, Andreas
Έκδοση 2009

Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis

ανά Najafi, Kimia, Kariminejad, Roxana, Hosseini, Kaveh, Moshtagh, Azadeh, Abbassi, Gole Maryam, Sadatian, Neda, Bazrgar, Masood, Kariminejad, Ariana, Kariminejad, Mohamad Hassan
Τόπος έκδοσης Case Rep Genet (2017)

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18

ανά Kariminejad, Ariana, Kariminejad, Roxana, Moshtagh, Azadeh, Zanganeh, Maryam, Kariminejad, Mohammad Hassan, Neuenschwander, Stefan, Okoniewski, Michal, Wey, Eva, Schinzel, Albert, Baumer, Alessandra
Έκδοση 2011

A Defect in the TUSC3 Gene Is Associated with Autosomal Recessive Mental Retardation

ανά Garshasbi, Masoud, Hadavi, Valeh, Habibi, Haleh, Kahrizi, Kimia, Kariminejad, Roxana, Behjati, Farkhondeh, Tzschach, Andreas, Najmabadi, Hossein, Ropers, Hans Hilger, Kuss, Andreas Walter
Έκδοση 2008

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

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

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

ανά Najafi, Kimia, Gholami, Soheila, Moshtagh, Azadeh, Bazrgar, Masood, Sadatian, Neda, Abbasi, Golemaryam, Rostami, Parvin, Khalili, Soheila, Babanejad, Mojgan, Nourmohammadi, Bahareh, Faramarzi Garous, Negin, Najmabadi, Hossein, Kariminejad, Roxana
Τόπος έκδοσης Mol Genet Genomic Med (2019)

Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3

ανά Kahrizi, Kimia, Hu, Cougar Hao, Garshasbi, Masoud, Abedini, Seyedeh Sedigheh, Ghadami, Shirin, Kariminejad, Roxana, Ullmann, Reinhard, Chen, Wei, Ropers, H-Hilger, Kuss, Andreas W, Najmabadi, Hossein, Tzschach, Andreas
Έκδοση 2011

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

ανά 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
Έκδοση 2011

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

ανά 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
Τόπος έκδοσης Int J Mol Cell Med (2016)

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

ανά 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
Τόπος έκδοσης Cell J (2019)

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

ανά 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
Έκδοση 2013

Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

ανά Kuechler, Alma, Zink, Alexander M, Wieland, Thomas, Lüdecke, Hermann-Josef, Cremer, Kirsten, Salviati, Leonardo, Magini, Pamela, Najafi, Kimia, Zweier, Christiane, Czeschik, Johanna Christina, Aretz, Stefan, Endele, Sabine, Tamburrino, Federica, Pinato, Claudia, Clementi, Maurizio, Gundlach, Jasmin, Maylahn, Carina, Mazzanti, Laura, Wohlleber, Eva, Schwarzmayr, Thomas, Kariminejad, Roxana, Schlessinger, Avner, Wieczorek, Dagmar, Strom, Tim M, Novarino, Gaia, Engels, Hartmut
Τόπος έκδοσης Eur J Hum Genet (2015)