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

por Ouldim, Karim, Natiq, Abdelhafid, Jonveaux, Philippe, Sefiani, Abdelaziz
Publicado 2007

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 2012

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 2014

Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report

por Amasdl, Saadia, Natiq, Abdelhafid, Elalaoui, Siham Chafai, Sbiti, Aziza, Liehr, Thomas, Sefiani, Abdelaziz
Publicado 2016

Near tetrapoloid karyotype with translocation t(11;14) in a Moroccan patient with amyloid light-chain amyloidosis and multiple myeloma

por Hamdaoui, Hasna, Natiq, Abdelhafid, Benlarroubia, Oumaima, Liehr, Thomas, Dehbi, Hind, Loukhmas, Latifa, Chegdani, Fatima
Publicado 2020

A new case of de novo 19p13.2p13.12 deletion in a girl with overgrowth and severe developmental delay

por Natiq, Abdelhafid, Elalaoui, Siham Chafai, Miesch, Sevrine, Bonnet, Celine, Jonveaux, Philippe, Amzazi, Saaïd, Sefiani, Abdelaziz
Publicado 2014

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature

por Amasdl, Saadia, Natiq, Abdelhafid, Sbiti, Aziza, Zerkaoui, Maria, Lyahyai, Jaber, Amzazi, Saaid, Liehr, Thomas, Sefiani, Abdelaziz
Publicado 2016

Autosomal Dominant Intellectual Development Disorder-6 (MRD6) Without Seizures Linked to a De Novo Mutation in the grin2b Gene Revealed by Exome Sequencing: A Case Report of a Moro...

por El Mouhi, Hinde, Abbassi, Meriame, Sayel, Hanane, Trhanint, Said, Natiq, Abdelhafid, El Hejjioui, Brahim, Jalte, Merym, Ahmadi, Youssef, Chaouki, Sana
Publicado 2023