A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report
Smaili, W, Elalaoui, S Chafai, Meier, S, Zerkaoui, M, Sefiani, A, Heinimann, K
Published in BMC medical genetics (03.05.2017)
Published in BMC medical genetics (03.05.2017)
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Journal Article
Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic features
Smaili, W., Elalaoui, S. Chafai, Zrhidri, A., Raymond, L., Egéa, G., Taoudi, M., Mouatassim, S.E.L., Sefiani, A., Lyahyai, J.
Published in European journal of medical genetics (01.07.2020)
Published in European journal of medical genetics (01.07.2020)
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Journal Article
CALR gene mutational profile in myeloproliferative neoplasms with non-mutated JAK2 in Moroccan patients: A case series and germline in-frame deletion
Smaili, W., Doubaj, Y., Laarabi, F.Z., Lyahyai, J., Kerbout, M., Mikdame, M., Sefiani, A.
Published in Current research in translational medicine (01.01.2017)
Published in Current research in translational medicine (01.01.2017)
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Journal Article