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Kheirie Issa

Children's Hospital of Eastern Ontario

4

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Evaluating Curricular Modules in the Care of Children with Medical Complexity: A Mixed-Methods Randomized Controlled Trial

2018 Academic Pediatrics
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Congenital sucrase—isomaltase deficiency: identification of a common Inuit founder mutation

2015 Canadian Medical Association Journal
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Atypical fibrodysplasia ossificans progressiva diagnosed by whole‐exome sequencing

2015 American Journal of Medical Genetics Part A
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MG-107 Congenital sucrase-isomaltase deficiency: Identification of the common inuit founder mutation

2015 Journal of Medical Genetics
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