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Heart, Lung & Circulation|February 12, 2020
Pre-Test Probability and Genes and Variants of Uncertain Significance in Familial Long QT SyndromeKathryn E Waddell-Smith, Jonathan R Skinner, J Martijn Bos
Molecular Medicine Reports|June 15, 2013
Bacterial artificial chromosomes (BACs)-on-Beads™ as a diagnostic platform for the rapid aneuploidy screening of products of conceptionKaren L Sheath, Lisa Duffy, Philip Asquith, et al.
Case Reports in Genetics|July 11, 2013
Delineation of 2q32q35 deletion phenotypes: two apparent "proximal" and "distal" syndromesAdrian Mc Cormack, Juliet Taylor, Nerine Gregersen, et al.
Sultan Qaboos University Medical Journal|July 18, 2013
Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental DelayRoberto L Mazzaschi, Fern Ashton, Salim Aftimos, et al.
Case Reports in Genetics|October 18, 2012
Amino-Terminal Microdeletion within the CNTNAP2 Gene Associated with Variable Expressivity of Speech DelayAmel Al-Murrani, Fern Ashton, Salim Aftimos, et al.
Heart, Lung & Circulation|August 7, 2022
Cultural Differences in Psychological Distress and Illness Perceptions Amongst People Living With Cardiac Inherited DiseasesJessee Fia'Ali'i, Mikaela Law, Claire O'Donovan, et al.
Journal of Law and Medicine|July 7, 2018
Use of Coronial Post-mortem Tissue for Research in New ZealandBrandi L Bellissima, Fintan Garavan, Jonathan R Skinner, et al.
Archives of Disease in Childhood|April 22, 2019
Fascicular tachycardia in infancy and the use of verapamil: a case series and literature reviewJascha Kehr, Alex Binfield, Fraser Maxwell, et al.
The Annals of Thoracic Surgery|March 20, 2003
Extracardiac conduit with a limited maze procedure for the failing Fontan with atrial tachycardiasShaun P Setty, Kirsten Finucane, Jonathan R Skinner, et al.
Psychology & Health|August 1, 2022
Perspectives and experiences of Māori and Pasifika peoples living with cardiac inherited disease: a qualitative studyJessee Fia'Ali'i, Mikaela Law, Claire O'Donovan, et al.
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