A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review by Mohammad Jahanpanah, Diana Mokhtari, Haleh Mokaber, Sara Arish, Farzad Ahmadabadi, Behzad Davarnia

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Genetic insights into congenital hypothyroidism in three Iranian Azeri families with consanguineous marriage: the role of novel and recurrent TPO gene variations by Mehrdad Mirzarahimi, Mohammad Panahi, Bahareh Rahimi, Ehsan Abbaspour Rodboneh, Shadi Abkhiz, Tannaz Fattahi, Sara Arish, Behzad Davarnia

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Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes by Diana Mokhtari, Mohammad Jahanpanah, Nasim Jabbari, Hamed Azari, Sana Davarnia, Haleh Mokaber, Sara Arish, Rasol Molatefi, Vahid Abbasi, Behzad Davarnia

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Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran by Marzieh Mohseni, Farzane Zare Ashrafi, Ehsan Abbaspour Rodbaneh, Haleh Mokabber, Maryam Vafaei, Ramiz Nobakht, Fatemeh Keshavarzi, Sanaz Arzhangi, Sara Arish, Zahra Nematollahi Azar, Kimia Kahrizi, Hossein Najmabadi, Behzad Davarnia

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