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Genetic Investigation of an Iranian Supercentenarian by Whole Exome Sequencing.

Autor: Akhtarkhavari, Tara¹, Joghataei, Mohammad Taghi², Fattahi, Zohreh¹, Akbari, Mohammad Reza³, Larti, Farzaneh¹, Najmabadi, Hossein¹, Kahrizi, Kimia¹ kahrizi@yahoo.com

Publikováno v: Archives of Iranian Medicine (AIM). Oct2015, Vol. 18 Issue 10, p688-697. 10p.

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Comprehensive genotype‐phenotype correlation in AP‐4 deficiency syndrome; Adding data from a large cohort of Iranian patients.

Autor: Beheshtian, Maryam, Akhtarkhavari, Tara, Mehvari, Sepideh, Mohseni, Marzieh, Fattahi, Zohreh, Abedini, Seyedeh Sedigheh, Arzhangi, Sanaz, Fadaee, Mahsa, Jamali, Payman, Najafipour, Reza, Kalscheuer, Vera M., Hu, Hao, Ropers, Hans‐Hilger, Najmabadi, Hossein, Kahrizi, Kimia

Publikováno v: Clinical Genetics; Jan2021, Vol. 99 Issue 1, p187-192, 6p

Emerging Epidemiological Data on Rare Intellectual Disability Syndromes from Analyzing the Data of a Large Iranian Cohort.

Autor: Zare Ashrafi F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Akhtarkhavari T; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Asadnezhad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Beheshtian M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Arzhangi S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

Publikováno v: Archives of Iranian medicine [Arch Iran Med] 2023 Apr 01; Vol. 26 (4), pp. 186-197. Date of Electronic Publication: 2023 Apr 01.