Mustapha El Alloussi
Rabat, Morocco
Last Updated: 09/26/2026
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Found 13 publications
Craniofacial Radiographic Features in Amelogenesis Imperfecta: A Case-Control Study.
Journal: Cureus
Published: November 09, 2025
Novel variant related to SATB2-associated syndrome.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: June 20, 2024
Oligodontia and Facial Phenotype Associated with a Rare Syndrome.
Journal: Case reports in dentistry
Published: March 03, 2022
Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.
Journal: Balkan journal of medical genetics : BJMG
Published: September 21, 2020
Novel splice site mutation in CNNM4 gene in a family with Jalili syndrome.
Journal: European journal of medical genetics
Published: October 19, 2016
Amelogenesis Imperfecta: 1 Family, 2 Phenotypes, and 2 Mutated Genes.
Journal: Journal of dental research
Published: August 26, 2016
Enamel-renal syndrome with congenital heart defects and asthma: a rare association in a Moroccan child.
Journal: Clinical dysmorphology
Published: August 20, 2016
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
Journal: Journal of medical genetics
Published: June 06, 2015
A rare association--amelogenesis imperfecta, platispondyly and bicytopenia: a case report.
Journal: Journal of medical case reports
Published: May 06, 2015
Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6.
Journal: American journal of human genetics
Published: April 24, 2015
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
Journal: BMC oral health
Published: September 21, 2014
Last Updated: 09/26/2026