Somayeh Takrim Nojehdeh
2PUBLICATIONS
5CO-AUTHORS
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Publications (2)
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|Dec 26, 2025
Partial Monosomy 21q Due to De Novo t(15;21)(q26.3;q22.11): A Case Report with Clinical and Molecular Findings.Somayeh Takrim Nojehdeh, Tannaz Fattahi, Sara Arish
|Dec 14, 2022
Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation.Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman
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