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Search Results - Basalom, Shuaa
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No, it is not mutually exclusive! A case report of a girl with two genetic diagnoses: Craniofrontonasal dysplasia and pontocerebellar hypoplasia type 1B
by
Ibrahim, Iman
,
Scriver, Tara
,
Basalom, Shuaa A.
Published in
Clinical case reports
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P318: Ironing out the BPAN phenotypic spectrum: A report of three new BPAN cases and review of the literature
by
Goedhart, Caitlin
,
Basalom, Shuaa
,
Skinner, Stephanie
,
Brost, Caroline
Published in
Genetics in Medicine Open
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Bone Disease in Patients with Ehlers–Danlos Syndromes
by
Basalom, Shuaa
,
Rauch, Frank
Published in
Current osteoporosis reports
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Variable expressivity in a family with an aggrecanopathy
by
Denis, Antoine
,
Chergui, Sami
,
Basalom, Shuaa
,
Campeau, Philippe M.
,
Janelle, Chantal
,
Pauyo, Thierry
Published in
Molecular genetics & genomic medicine
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Calvarial doughnut lesions with bone fragility in a French-Canadian family; case report and review of the literature
by
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.
Published in
BONE REPORTS
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Dyssegmental dysplasia, Silverman‐Handmaker type: A challenging antenatal diagnosis in a dizygotic twin pregnancy
by
Basalom, Shuaa
,
Trakadis, Yannis
,
Shear, Roberta
,
Azouz, Michel E.
,
De Bie, Isabelle
Published in
Molecular genetics & genomic medicine
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Calvarial doughnut lesions with bone fragility in a French-Canadian family; case report and review of the literature
by
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
Published in
Bone reports
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