受强制性开放获取政策约束的文章 - Dor mohammad Kordi -Tammandani, Professor of Molecular Genetics了解详情
可在其他位置公开访问的文章：3 篇
Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis
M Najafi, DM Kordi-Tamandani, F Behjati, S Sadeghi-Bojd, Z Bakey, ...
Orphanet journal of rare diseases 14, 1-11, 2019
强制性开放获取政策： German Research Foundation, European Commission
A 57 kB Genomic Deletion Causing CTNS Loss of Function Contributes to the CTNS Mutational Spectrum in the Middle East
M Najafi, DMK Tamandani, A Azarfar, Z Bakey, F Behjati, D Antony, ...
Frontiers in pediatrics 7, 89, 2019
强制性开放获取政策： German Research Foundation, European Commission
Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update
T Baranzehi, DM Kordi-Tamandani, M Najafi, A Khajeh, M Schmidts
Journal of Clinical Medicine 11 (21), 6415, 2022
强制性开放获取政策： German Research Foundation, European Commission
出版信息和资助信息由计算机程序自动确定