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Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation.
Behjati F, Ghasemi Firouzabadi S, Sajedi F, Kahrizi K, Najafi M, Ebrahimizade Ghasemlou B, Shafeghati Y, Behnia F, Mohammadi Arya AR, Karimi H, Hadipour F, Hadipour Z, Jamali P, Kariminejad R, Darvish H, Bahman I, Bagherizadeh E, Najmabadi H, Vameghi R. Behjati F, et al. Among authors: hadipour f, hadipour z. Iran Red Crescent Med J. 2013 Oct;15(10):e8221. doi: 10.5812/ircmj.8221. Epub 2013 Oct 5. Iran Red Crescent Med J. 2013. PMID: 24693374 Free PMC article.
Investigation of Chromosomal Abnormalities and Microdeletion/ Microduplication(s) in Fifty Iranian Patients with Multiple Congenital Anomalies.
Mohammadzadeh A, Akbaroghli S, Aghaei-Moghadam E, Mahdieh N, Badv RS, Jamali P, Kariminejad R, Chavoshzadeh Z, Ghasemi Firouzabadi S, Mansour Ghanaie R, Nozari A, Banihashemi S, Hadipour F, Hadipour Z, Kariminejad A, Najmabadi H, Shafeghati Y, Behjati F. Mohammadzadeh A, et al. Among authors: hadipour f. Cell J. 2019 Oct;21(3):337-349. doi: 10.22074/cellj.2019.6053. Epub 2019 Jun 15. Cell J. 2019. PMID: 31210441 Free PMC article.
Whole-Exome Sequencing Identifies Three Candidate Homozygous Variants in a Consanguineous Iranian Family with Autism Spectrum Disorder and Skeletal Problems.
Farajzadeh Valilou S, Alavi A, Pashaei M, Ghasemi Firouzabadi S, Shafeghati Y, Nozari A, Hadipour F, Hadipour Z, Maghsoodlou Estrabadi B, Gholamreza Noorazar S, Banihashemi S, Karimian J, Fattahi M, Behjati F. Farajzadeh Valilou S, et al. Among authors: hadipour f. Mol Syndromol. 2020 Jun;11(2):62-72. doi: 10.1159/000506530. Epub 2020 Mar 11. Mol Syndromol. 2020. PMID: 32655337 Free PMC article.
Inborn Errors of Metabolism Associated With Autism Among Children: A Multicenter Study from Iran.
Moravej H, Inaloo S, Nahid S, Mazloumi S, Nemati H, Moosavian T, Nasiri J, Ghasemi F, Alaei MR, Dalili S, Aminzadeh M, Katibeh P, Amirhakimi A, Yazdani N, Ilkhanipoor H, Afshar Z, Hadipour F, Hadipour Z. Moravej H, et al. Among authors: hadipour f. Indian Pediatr. 2023 Mar 15;60(3):193-196. Epub 2023 Jan 2. Indian Pediatr. 2023. PMID: 36604934 Free article.
The genomic architecture of NLRP7 is Alu rich and predisposes to disease-associated large deletions.
Reddy R, Nguyen NM, Sarrabay G, Rezaei M, Rivas MC, Kavasoglu A, Berkil H, Elshafey A, Abdalla E, Nunez KP, Dreyfus H, Philippe M, Hadipour Z, Durmaz A, Eaton EE, Schubert B, Ulker V, Hadipour F, Ahmadpour F, Touitou I, Fardaei M, Slim R. Reddy R, et al. Among authors: hadipour f. Eur J Hum Genet. 2016 Oct;24(10):1445-52. doi: 10.1038/ejhg.2016.9. Epub 2016 Mar 9. Eur J Hum Genet. 2016. PMID: 26956250 Free PMC article.
15 results