Syndrome de Silver Russell: à propos de 3 cas et revue de la litterature

Por Lamzouri, Afaf, Ratbi, Ilham, Sefiani, Abdelaziz
Publicado em 2013

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Por Aziza Sbiti, Fatiha El Kerch, Abdelaziz Sefiani
Publicado em 2002-01-01

Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Por Sbiti, Aziza, El Kerch, Fatiha, Sefiani, Abdelaziz
Publicado em 2002

The Moroccan human mutation database

Por Ratbi, Ilham, Gati, Alae-eddine, Sefiani, Abdelaziz
Publicado em 2008

Genetics and genomic medicine in Morocco: the present hope can make the future bright

Por Belhassan, Khadija, Ouldim, Karim, Sefiani, Abdel Aziz
Publicado no Mol Genet Genomic Med (2016)

Autosomal recessive anhidrotic ectodermal dysplasia in a large Moroccan family.

Por Kabbaj, K, Baala, L, Chhoul, H, Sefiani, A
Publicado em 1998

Tetrasomy 15q11-q13 Diagnosed by FISH in a Patient with Autistic Disorder

Por Ouldim, Karim, Natiq, Abdelhafid, Jonveaux, Philippe, Sefiani, Abdelaziz
Publicado em 2007

Experimental implementation of a new multi input multi output fuzzy-PID controller in a poultry house system

Por Lahlouh, Ilyas, Rerhrhaye, Fathallah, Elakkary, Ahmed, Sefiani, Nacer
Publicado no Heliyon (2020)

A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report

Por Yassamine Doubaj, Wiam Smaili, Fatima-Zahra Laarabi, Abdelaziz Sefiani
Publicado em 2017-06-01

Hyaline fibromatosis syndrome with mutation c.1074delT of the CMG2 gene: a case report

Por Cherkaoui Jaouad, Imane, Guaoua, Soukaina, Hajjioui, Aicha, Sefiani, Abdelaziz
Publicado em 2014

A novel frameshift mutation in the XPC gene in a Moroccan patient: a case report

Por Doubaj, Yassamine, Smaili, Wiam, Laarabi, Fatima-Zahra, Sefiani, Abdelaziz
Publicado no J Med Case Rep (2017)

Le diagnostic anténatal de la trisomie 21 par l'hybridation in situ en fluorescence (FISH): à propos des premiers tests réalisés au Maroc

Por Lamzouri, Afaf, Natiq, Abdelhafid, Tajir, Mariam, Sendid, Mohamed, Sefiani, Abdelaziz
Publicado em 2012

P321: Current status of pharmacovigilance in Africa

Por Skalli, S, Sefiani, H, Soulaymani, R, Errkhis, R Ouled, Benkirane, R
Publicado em 2013

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene

Por Tajir, M, Lyahyai, J, Guaoua, S, El Alloussi, M, Sefiani, A
Publicado no Balkan J Med Genet (2020)

Best strategy in managing the association of Horse-shoe-Kidney and Abdominal Aortic Aneurysm: Case report

Por Bounssir, Ayoub, Bakkali, Tarik, Taghi, Houda, Sefiani, Yasser, Lekehal, Brahim
Publicado no Int J Surg Case Rep (2020)

A novel single variant in the MEFV gene causing Mediterranean fever and Behçet’s disease: a case report

Por Maria Zerkaoui, Fatima Zahra Laarabi, Yousra Ajhoun, Bouchra Chkirate, Abdelaziz Sefiani
Publicado em 2018-03-01

A recurrent mutation in Moroccan patients with Dyggve-Melchior-Clausen syndrome: Report of a new case and review

Por Elalaoui, Siham Chafai, Mariam, Tajir, Ilham, Ratbi, Yassamine, Doubaj, Abdelaziz, Sefiani
Publicado em 2011

Maternal Hypomethylation of KvDMR in a Monozygotic Male Twin Pair Discordant for Beckwith-Wiedemann Syndrome

Por Elalaoui, S.C., Garin, I., Sefiani, A., Perez de Nanclares, G.
Publicado em 2014

Characterization of a rare short arm heteromorphism of chromosome 22 in a girl with down-syndrome like facies

Por Natiq, Abdelhafid, Elalaoui, Siham Chafai, Liehr, Thomas, Amzazi, Saïd, Sefiani, Abdelaziz
Publicado em 2014

A novel TRPS1 mutation in a Moroccan family with Tricho-rhino-phalangeal syndrome type III: case report

Por Smaili, W., Elalaoui, S. Chafai, Meier, S., Zerkaoui, M., Sefiani, A., Heinimann, K.
Publicado no BMC Med Genet (2017)