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| Preview | Issue Date | Title | Author(s) |
| 2017 | Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations | Corbett, M.; Turner, S.; Gardner, A.; Silver, J.; Stankovich, J.; Leventer, R.; Derry, C.; Carroll, R.; Ha, T.; Scheffer, I.; Bahlo, M.; Jackson, G.; Mackey, D.; Berkovic, S.; Gecz, J. |
| 1998 | Febrile seizures and generalised epilepsy associated with a mutation in the Na+-channel b1 subunit gene SCN1B | Wallace, R.; Wang, D.; Singh, R.; Scheffer, I.; George Jnr., A.; Phillips, H.; Saar, K.; Reis, A.; Johnson, E.; Sutherland, G.; Berkovic, S.; Mulley, J. |
| 1999 | Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient | Gecz, J.; Baker, E.; Donnelly, A.; Ming, J.; McDonald-McGinn, D.; Spinner, N.; Zackai, E.; Sutherland, G.; Mulley, J. |
| 2015 | Fiddling with the proof: the Magpie Fiddler Ray is a colour pattern variant of the common Southern Fiddler Ray (Rhinobatidae: Trygonorrhina) | Donnellan, S.; Foster, R.; Junge, C.; Huveneers, C.; Rogers, P.; Kilian, A.; Bertozzi, T. |
| 2014 | Fifty thousand years of Arctic vegetation and megafaunal diet | Willerslev, E.; Davison, J.; Moora, M.; Zobel, M.; Coissac, E.; Edwards, M.; Lorenzen, E.; Vestergård, M.; Gussarova, G.; Haile, J.; Craine, J.; Gielly, L.; Boessenkool, S.; Epp, L.; Pearman, P.; Cheddadi, R.; Murray, D.; Bråthen, K.; Yoccoz, N.; Binney, H.; et al. |
| 2015 | First comparative insight into the architecture of COI mitochondrial minicircle molecules of dicyemids reveals marked inter-species variation | Catalano, S.; Whittington, I.; Donnellan, S.; Bertozzi, T.; Gillanders, B. |
| 2014 | Fitness valleys constrain HIV-1's adaptation to its secondary chemokine coreceptor | Da Silva, J.; Wyatt, S. |
| 2021 | Flavors of non-random meiotic segregation of autosomes and sex chromosomes | Pajpach, F.; Wu, T.; Shearwin, L.; Jones, K.; Grutzner, F. |
| 2000 | Fly methods for the new millennium | Gregory, S.L. |
| 2015 | Forensic timber identification: it's time to integrate disciplines to combat illegal logging | Dormontt, E.; Boner, M.; Braun, B.; Breulmann, G.; Degen, B.; Espinoza, E.; Gardner, S.; Guillery, P.; Hermanson, J.; Koch, G.; Lee, S.; Kanashiro, M.; Rimbawanto, A.; Thomas, D.; Wiedenhoeft, A.; Yin, Y.; Zahnen, J.; Lowe, A. |
| 1996 | Fragile X Syndrome and other X-linked Causes of Mental Handicap | Sutherland, G.; Mulley, J. |
| 1995 | FRAXE and mental retardation | Mulley, J.; Yu, S.; Loesch, D.; Hay, D.; Donnelly, A.; Gedeon, A.; Carbonell, P.; Lopez, I.; Glover, G.; Garbarron, I.; Yu, P.; Baker, E.; Haan, E.; Hockey, A.; Knight, S.; Daview, K.; Richards, R.; Sutherland, G. |
| 2014 | From cheek swabs to consensus sequences: an A to Z protocol for high-throughput DNA sequencing of complete human mitochondrial genomes | Clarke, A.; Prost, S.; Stanton, J.; White, W.; Kaplan, M.; Matisoo-Smith, E.; Genographic Consortium, |
| 2017 | Functional equivalence of the SOX2 and SOX3 transcription factors in the developing mouse brain and testes | Adikusuma, F.; Pederick, D.; McAninch, D.; Hughes, J.; Thomas, P. |
| 1999 | FXY2/MID2, a gene related to the X-linked Opitz Syndrome gene FXY/MID1, maps to Xq22 and encodes a FNIII domain-containing protein that associates with microtubules | Perry, J.; Short, K.; Romer, J.; Swift, S.; Cox, T.; Ashworth, A. |
| 2014 | Gasteruption youngi sp. nov. (Hymenoptera: Evanioidea: Gasteruptiidae) from South Australia; an unusual species with trichoid sensilla on the ovipositor sheaths | Jennings, J.; Parslow, B. |
| 2018 | Gene expression drives the evolution of dominance | Huber, C.D.; Durvasula, A.; Hancock, A.M.; Lohmueller, K.E. |
| 1998 | Gene localisation for an autosomal dominant familial periodic fever to 12p13. | Mulley, J.; Saar, K.; Hewitt, G.; Rueschendorf, F.; Phillips, H.; Colley, A.; Sillence, D.; Reis, A.; Wilson, M. |
| 1996 | Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470) | Gedeon, A.; Haan, E.; Mulley, J. |
| 1996 | Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585) | Gedeon, A.; Turner, G.; Mulley, J. |
