No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B

por Ibrahim, Iman, Scriver, Tara, Basalom, Shuaa A.
Publicado 2023

Dyssegmental dysplasia, Silverman‐Handmaker type: A challenging antenatal diagnosis in a dizygotic twin pregnancy

por Basalom, Shuaa, Trakadis, Yannis, Shear, Roberta, Azouz, Michel E., De Bie, Isabelle
Publicado 2018

Variable expressivity in a family with an aggrecanopathy

por Denis, Antoine, Chergui, Sami, Basalom, Shuaa, Campeau, Philippe M., Janelle, Chantal, Pauyo, Thierry
Publicado 2021

Calvarial doughnut lesions with bone fragility in a French-Canadian family; case report and review of the literature

por Basalom, Shuaa, Fiscaletti, Mélissa, Miranda, Valancy, Huber, Céline, Couture, Guillaume, Drouin, Régen, Monceau, Élise, Wavrant, Sandrine, Dubé, Johanne, Mäkitie, Outi, Cormier-Daire, Valérie, Campeau, Philippe M.
Publicado 2021