Lockhart, Paul J
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Payne, Jonathan M ORCID: 0000-0001-9565-3845, Haebich, Kristina M, Mitchell, Rebecca ORCID: 0000-0001-9783-3495, Bozaoglu, Kiymet ORCID: 0000-0002-0807-2813, Giliberto, Emma, Lockhart, Paul J ORCID: 0000-0003-2531-8413, Maier, Alice, Velasco, Silvia ORCID: 0000-0003-0638-0932, Ball, Gareth ORCID: 0000-0003-3509-1435, North, Kathryn N and Hocking, Darren ORCID: 0000-0003-1143-8190 (2024) Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysis. Molecular psychiatry. ISSN 1359-4184
Delatycki, Martin B, Wolthuizen, Michelle, Collins, Veronica, Varley, Elizabeth, Craven, Joanna, Allen, Katrina J, Gurrin, Lyle, Aitken, Maryanne, Trembath, M Kaye, Bond, Lyndal ORCID: 0000-0003-1693-5508, Wilson, Gabrielle R, Stephenson, Sarah EM, Macciocca, Ivan, Hickerton, Chriselle, Lockhart, Paul J and Metcalfe, Sylvia A (2012) ironXS: High-school screening for hereditary haemochromatosis is acceptable and feasible. European Journal of Human Genetics, 20 (5). 505 - 509. ISSN 1018-4813
Delatycki, Martin B, Wolthuizen, Michelle, Collins, Veronica, Varley, E, Craven, Joanna, Allen, Katrina J, Aitken, Maryanne, Bond, Lyndal ORCID: 0000-0003-1693-5508, Lockhart, Paul J, Wilson, Gabrielle R, Macciocca, Ivan and Metcalfe, Sylvia A (2010) Implementation of ironXS: A study of the acceptability and feasibility of genetic screening for hereditary hemochromatosis in high schools. Clinical Genetics, 77 (3). 241 - 248. ISSN 0009-9163