El Alloussi, Mustapha

Top Publications

Top Publications Authored or Co-Authored by "El Alloussi, Mustapha"

• Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6

  American Journal of Human Genetics, Volume 97, No. 4, Year 2015, Citations 101
• A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

  Journal of Medical Genetics, Volume 53, No. 2, Year 2015, Citations 101
• Amelogenesis Imperfecta: 1 Family, 2 Phenotypes, and 2 Mutated Genes

  Journal of Dental Research, Volume 95, No. 13, Year 2016, Citations 25
• A novel nonsense mutation in scn9a in a moroccan child with congenital insensitivity to pain

  Pediatric Neurology, Volume 51, No. 5, Year 2014, Citations 18
• Inhabitual autosomal recessive form of dentin dysplasia type I in a large consanguineous Moroccan family

  European Journal of Medical Genetics, Volume 56, No. 8, Year 2013, Citations 16