Behzad Davarnia
5PUBLICATIONS
6CO-AUTHORS
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Publications (5)
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|Jan 28, 2026
Identification of a Novel TBCK Variation in an Azari Consanguineous Family With Psychomotor Developmental Disorder.Sara Arish, Ramiz Nobakht, Haleh Mokabber
|Nov 14, 2025
Molecular Analysis of the HGD Gene in 9 Families With Alkaptonuric Ochronosis in Iran and Identification of Two Novel Variants.Ahad Azami, Mohammad Jahanpanah, Yousef Imani Marani
|Feb 19, 2025
Unraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran.Marzieh Mohseni, Farzane Zare Ashrafi, Ehsan Abbaspour Rodbaneh
|Mar 28, 2024
A novel variant in ASNS gene responsible for syndromic intellectual disability and microcephaly: Case report and literature review.Mohammad Jahanpanah, Diana Mokhtari, Haleh Mokaber
|Sep 28, 2021
GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran.Ehsan Abbaspour Rodbaneh, Mohammad Panahi, Bahareh Rahimi
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