M. Elalloussi

Severe early onset retinitis pigmentosa in a Moroccan patient with Heimler syndrome due to novel homozygous mutation of PEX1 gene.

W. Newman, J. Lyahyai, I. Jaouad, 2016, European journal of medical genetics.

Fixed Apparatus Medication of a Skeletal Class II Open Chomp Malocclusion with Hypomature Amelogenesis Blemished: Case Report

F. Zaoui, A. Sefiani, M. Elalloussi, 2013 .

DNA ligase IV deficiency: Immunoglobulin class deficiency depends on the genotype

A. Verloes, T. Leblanc, M. Doco‐Fenzy, 2017, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Non lethal Raine syndrome and differential diagnosis.

W. Newman, S. Bhaskar, J. Lyahyai, 2016, European journal of medical genetics.

The Hall Technique: A Non-conventional Method for Managing Carious Primary Molars

M. Elalloussi, M. Hariri, H. Ramdi, 2016 .