Ouldim, K.
Centre Hospitalier Universitaire Hassan II
2 papers on CoChatORCID 0000-0003-3974-5889
Most cited papers
- Verified
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
Bal, E., Baala, L., Cluzeau, C., El Kerch, F., Ouldim, K., Hadj-Rabia, S., Bodemer, C., Munnich, A., Courtois, G., Sefiani, A., et al. (2007) · Human Mutation
dental development and anomaliesGenetic and rare skin diseases.
Cited by 100
- Verified
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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