Benrhouma Hanene

Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome

T. Mazza, S. Castellana, E. Valente, 2014, Orphanet Journal of Rare Diseases.

Methylmalonic acidemia and hyperglycemia: An unusual association

Benrhouma Hanene, Marouani Imen, K. Ichraf, 2012, Brain and Development.