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