Samri, Imane

Centre Hospitalier Universitaire Hassan II

1 paper on CoChatORCID 0000-0002-2586-9015

Most cited papers

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Screening of NKX2.5 gene in Moroccan tetralogy of Fallot (TOF) patients: Worldwide mutation rate comparisons show a significant association between R25C variant and TOF phenotype
EL Bouchikhi, I., Belhassan, K., Moufid, F. Z., Bouguenouch, L., Samri, I., Iraqui Houssaïni, M., Ouldim, K., & Atmani, S. (2021) · Egyptian Journal of Medical Human Genetics
Congenital heart defects researchCongenital Heart Disease Studies
Cited by 4

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