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Conference Abstracts
, 2022, 'VP.02 Comprehensive characterization of early-onset skeletal muscle disease gene exon usage and splicing patterns across different developmental ages', in Neuromuscular Disorders, Elsevier, Vol. 32, pp. s47, http://dx.doi.org/10.1016/j.nmd.2022.07.027
, 2020, 'Biallelic and monoallelic variants in PLXNA1 cause a syndromic disorder with neurodevelopmental and oculo-cerebral anomalies', in EUROPEAN JOURNAL OF HUMAN GENETICS, SPRINGERNATURE, Vol. 28, pp. 130 - 131, https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000598482600236&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=891bb5ab6ba270e68a29b250adbe88d1
, 2020, 'NEW GENES AND DISEASES / NGS & RELATED TECHNIQUES P.334 Introme identifies non-canonical splice-altering variants in neuromuscular patients resulting in multiple new genetic diagnoses', in Neuromuscular Disorders, Elsevier, Vol. 30, pp. s144, http://dx.doi.org/10.1016/j.nmd.2020.08.330
, 2019, 'Penetrance of Dilated Cardiomyopathy in Families with Truncating TTN Variants: a National Perspective', in Heart Lung and Circulation, Elsevier, Vol. 28, pp. s140, http://dx.doi.org/10.1016/j.hlc.2019.06.019