Ahmad Ebrahimi
2PUBLICATIONS
18CO-AUTHORS
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Publications (2)
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|Sep 05, 2020
A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic Hearing Loss.Zahra Sadeghi, Seyedeh Parisa Chavoshi Tarzjani, Reyhaneh Sadat Miri Moosavi
|Feb 25, 2017
Rationale and Design of a Genetic Study on Cardiometabolic Risk Factors: Protocol for the Tehran Cardiometabolic Genetic Study (TCGS).Maryam S Daneshpour, Mohammad-Sadegh Fallah, Bahareh Sedaghati-Khayat
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Frequent Collaborators
1 joint publications
Maryam S Daneshpour
1 joint publications
Mohammad-Sadegh Fallah
1 joint publications
Bahareh Sedaghati-Khayat
1 joint publications
Kamran Guity
1 joint publications
Davood Khalili
1 joint publications
Mehdi Hedayati
1 joint publications
Farhad Hajsheikholeslami
1 joint publications
Parvin Mirmiran
1 joint publications
Fahimeh Ramezani Tehrani
1 joint publications
Amir-Abbas Momenan
