Publications by authors named "Fallon Noon"

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Correction to: A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.
Aimee Huynh, Paul E Gray, Anna Sullivan, Joseph Mackie, Antoine Guerin, Fallon Noon

J Clin Immunol· September 2024

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A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries.
Aimee Huynh, Paul E Gray, Anna Sullivan, Joseph Mackie, Antoine Guerin, Fallon Noon

J Clin Immunol· August 2024

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Biallellic variants in CACNA1S cause fetal akinesia sequence, progressive hydrops and stillbirth.
Emma Seed, Fallon Noon, Di Milnes, Tony Roscioli, Karl Kristensen

Prenat Diagn· December 2023

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