Biblio
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Filtres: Auteur is Mcdougall, Carey [Clear All Filters]
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2018. De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. AMERICAN JOURNAL OF HUMAN GENETICS. 103:305-316.
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2020. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor beta Signaling. BIOLOGICAL PSYCHIATRY. 87:100-112.
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2017. STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability. JOURNAL OF MEDICAL GENETICS. 54:479-488.