No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B von Ibrahim, Iman, Scriver, Tara, Basalom, Shuaa A.

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Bone Disease in Patients with Ehlers–Danlos Syndromes von Basalom, Shuaa, Rauch, Frank

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P318: Ironing out the BPAN phenotypic spectrum: A report of three new BPAN cases and review of the literature von Goedhart, Caitlin, Basalom, Shuaa, Skinner, Stephanie, Brost, Caroline

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

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Variable expressivity in a family with an aggrecanopathy von Denis, Antoine, Chergui, Sami, Basalom, Shuaa, Campeau, Philippe M., Janelle, Chantal, Pauyo, Thierry

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Dyssegmental dysplasia, Silverman‐Handmaker type: A challenging antenatal diagnosis in a dizygotic twin pregnancy von Basalom, Shuaa, Trakadis, Yannis, Shear, Roberta, Azouz, Michel E., De Bie, Isabelle

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

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