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PreviewIssue DateTitleAuthor(s)
2022The phenotypic spectrum of ADAMTSL4-associated ectopia lentis: Additional cases, complications, and review of literatureKnight, L.S.W.; Mullany, S.; Taranath, D.A.; Ruddle, J.B.; Barnett, C.P.; Sallevelt, S.C.E.H.; Berry, E.C.; Marshall, H.N.; Hollitt, G.L.; Souzeau, E.; Craig, J.E.; Siggs, O.M.
2000Phylogenetic relationships of human populations in sub-Saharan AfricaWeber, W.; Nash, D.; Motulsky, A.; Henneberg, M.; Crawford, M.; Martin, S.; Goldsmid, J.; Spedini, G.; Glidewell, S.; Schanfield, M.
2017A genetic screen for impaired systemic RNAi highlights the crucial role of DICER-LIKE 2Taochy, C.; Gursanscky, N.; Cao, J.; Fletcher, S.; Dressel, U.; Mitter, N.; Tucker, M.; Koltunow, A.; Bowman, J.; Vaucheret, H.; Carroll, B.
1998X-linked adrenoleukodystrophy: the Australasian experienceKirk, E.; Fletcher, J.; Sharp, P.; Carey, B.; Poulos, A.
2013Common variants in mendelian kidney disease genes and their association with renal functionParsa, A.; Fuchsberger, C.; Köttgen, A.; O'Seaghdha, C.; Pattaro, C.; De Andrade, M.; Chasman, D.; Teumer, A.; Endlich, K.; Olden, M.; Chen, M.; Tin, A.; Kim, Y.; Taliun, D.; Li, M.; Feitosa, M.; Gorski, M.; Yang, Q.; Hundertmark, C.; Foster, M.; et al.
1997Unbalanced t(4;11)(q32-q23) in a 34-year-old man with manifestations of distal monosomy 11q and trisomy 4q syndromesByatt, S.; Baker, E.; Richards, R.; Roberts, C.; Smith, A.
2004ABO genotyping by PCR-RFLP and cloning and sequencingHaak, W.; Burger, J.; Alt, K.
2019Australian adults with bronchiectasis: the first report from the Australian Bronchiectasis RegistryVisser, S.K.; Bye, P.T.P.; Fox, G.J.; Burr, L.D.; Chang, A.B.; Holmes-Liew, C.L.; King, P.; Middleton, P.G.; Maguire, G.P.; Smith, D.; Thomson, R.M.; Stroil-Salama, E.; Britton, W.J.; Morgan, L.C.
2020Definition and diagnosis of cerebral palsy in genetic studies: a systematic reviewPham, R.; Mol, B.W.; Gecz, J.; MacLennan, A.H.; MacLennan, S.C.; Corbett, M.A.; van Eyk, C.L.; Webber, D.L.; Palmer, L.J.; Berry, J.G.
2017An immunogenic phenotype in paternal antigen-specific CD8⁺ T cells at embryo implantation elicits later fetal loss in miceMoldenhauer, L.; Diener, K.; Hayball, J.; Robertson, S.

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