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PreviewIssue DateTitleAuthor(s)
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
1995An integrated physical map of human chromosome 16Doggett, N.; Goodwin, L.; Tesmer, J.; Meincke, L.; Bruce, D.; Clark, L.; Altherr, M.; Ford, A.; Chi, H.C.; Marrone, B.; Longmire, J.; Lane, S.; Whitmore, S.; Lowenstein, N.; Sutherland, G.; Mundt, M.; Knill, E.; Bruno, W.; Macken, C.; Torney, D.; et al.
2007Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countriesRescorla, L.; Achenbach, T.; Ivanova, M.; Dumenci, L.; Almqvist, F.; Bilenberg, N.; Bird, H.; Broberg, A.; Dobrean, A.; Dopfner, M.; Erol, N.; Forns, M.; Hannesdottir, H.; Kanbayashi, Y.; Lambert, M.; Leung, P.; Minaei, A.; Mulatu, M.; Novik, T.; Oh, K.; et al.
1997A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndromeMuenke, M.; Gripp, K.; McDonald-McGinn, D.; Gaudenz, K.; Whitaker, L.; Bartlett, S.; Markowitz, R.; Robin, N.; Nwokoro, N.; Mulvihill, J.; Losken, H.; Mulliken, J.; Guttmacher, A.; Wilroy, R.; Clarke, L.; Hollway, G.; Ades, L.; Haan, E.; Mulley, J.; Cohen, M.; et al.
2007The Women's international study of long-duration oestrogen after menopause (WISDOM): a randomised controlled trialVickers, M.; Martin, J.; Meade, T.; Wilkes, H.; Ford, D.; Walgrove, A.; Arasaratnum, N.; Collins, N.; Furness, P.; Ghali, M.; Gordon, E.; Huppert, F.; Islam, Z.; Knott, C.; Meredith, S.; Prince, M.; Purdon, S.; Richards, M.; Taylor, L.; Welton, A.; et al.
2007Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitusRaymond, F.; Tarpey, P.; Edkins, S.; Tofts, C.; O'Meara, S.; Teague, J.; Butler, A.; Stevens, C.; Barthorpe, S.; Buck, G.; Cole, J.; Dicks, E.; Gray, K.; Harrison, R.; Hills, K.; Hinton, J.; Jones, D.; Menzies, A.; Perry, J.; Raine, K.; et al.
2018The impact of the 13 valent conjugate pneumococcal vaccine on pneumococcal serotypes causing childhood empyema in AustraliaStrachan, R.; Beggs, S.; Fearon, D.; Gilbert, G.; Homaira, N.; Lambert, S.; Marshall, H.; Martin, A.; McCallum, G.; McCullagh, A.; McDonald, T.; Mcintyre, P.; Oftadeh, S.; Ranganathan, S.; Suresh, S.; Teoh, L.; Twaij, A.; Wainwright, C.; Wong, M.; Snelling, T.; et al.; The Australia & New Zealand Society of Respiratory Science and The Thoracic Society of Australia and New Zealand (ANZSRS/TSANZ) Annual Scientific Meeting 2018 (23 Mar 2018 - 27 Mar 2018 : Adelaide, AUSTRALIA)
2014The inherited cancer connect (iccon) mutation-carrier databaseJames, P.A.; Petelin, L.; Campbell, I.; Dawkins, H.; Fox, S.; Hiller, J.; Kirk, J.; Lindeman, G.; Macrae, F.; Mascarenhas, L.; McGaughran, J.; Meiser, B.; Morrow, A.; Nichols, C.; Pachter, N.; Saunders, C.; Scott, C.; Poplawski, N.; Thrupp, L.; Trainer, A.; et al.; COSA's 41st Annual Scientific Meeting. Joining Forces - Accelerating Progress (2 Dec 2014 - 4 Dec 2014 : Melbourne, Vic.)
2020Septum resection in women with a septate uterus: a cohort studyRikken, J.F.; Verhorstert, K.W.; Emanuel, M.H.; Kuchenbecker, W.K.; Jansen, F.W.; Torrenga, B.; Schols, W.A.; Verhoeve, H.R.; Hoek, A.; Clark, T.J.; Stephenson, M.; Mol, B.W.; Van der Veen, F.; Van Wely, M.; Goddijn, M.; Bongers, M.Y.; van der Steeg, J.W.; Janssen, I.A.H.; Kapiteijn, K.; Torrance, H.L.; et al.
2019Septum resection in women with a septate uterus: a cohort studyRikken, J.F.; Verhorstert, K.W.; Emanuel, M.H.; Kuchenbecker, W.K.; Jansen, F.W.; Torrenga, B.; Schols, W.A.; Verhoeve, H.R.; Hoek, A.; Clark, T.J.; Stephenson, M.; Mol, B.W.; Van der Veen, F.; Van Wely, M.; Goddijn, M.; Bongers, M.Y.; van der Steeg, J.W.; Janssen, I.A.H.; Kapiteijn, K.; Torrance, H.L.; et al.; Annual Meeting of the European Society of Human Reproduction and Embryology (ESHRE) (24 Jun 2019 - 26 Jun 2019 : Vienna, AUSTRIA)

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