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Results 1-10 of 11 (Search time: 0.007 seconds).
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Issue Date
Title
Author(s)
1997
Genomic structure and complete nucleotide sequence of the Batten Disease Gene, CLN3
Mitchison, H.
;
Munroe, P.
;
O'Rawe, A.
;
Taschner, P.
;
De Vos, N.
;
Kremmidiotis, G.
;
Lensink, I.
;
Munk, A.
;
D'Arigo, K.
;
Anderson, J.
;
Lerner, T.
;
Moyzis, R.
;
Callen, D.
;
Breuning, M.
;
Doggett, N.
;
Gardiner, R.
;
Mole, S.
1998
Construction of an ~700-kb transcript map around the Familial Mediterranean Fever locus on human chromosome 16p13.3
Centola, M.
;
Chen, X.
;
Sood, R.
;
Deng, Z.
;
Aksentijevich, I.
;
Blake, T.
;
Ricke, D.
;
Chen, X.
;
Wood, G.
;
Zaks, N.
;
Richards, N.
;
Krizman, D.
;
Mansfield, E.
;
Apostolou, S.
;
Liu, J.
;
Shafran, N.
;
Vedula, A.
;
Hamon, M.
;
Cercek, A.
;
Kahan, T.
;
et al.
2019
Race in a genome: long read sequencing, ethnicity-specific reference genomes and the shifting horizon of race
Kowal, E.
;
Llamas, B.
2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing
Jansen, I.E.
;
Ye, H.
;
Heetveld, S.
;
Lechler, M.C.
;
Michels, H.
;
Seinstra, R.I.
;
Lubbe, S.J.
;
Drouet, V.
;
Lesage, S.
;
Majounie, E.
;
Gibbs, J.R.
;
Nalls, M.A.
;
Ryten, M.
;
Botia, J.A.
;
Vandrovcova, J.
;
Simon-Sanchez, J.
;
Castillo-Lizardo, M.
;
Rizzu, P.
;
Blauwendraat, C.
;
Chouhan, A.K.
;
et al.
2020
Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia
Marcus, J.H.
;
Posth, C.
;
Ringbauer, H.
;
Lai, L.
;
Skeates, R.
;
Sidore, C.
;
Beckett, J.
;
Furtwängler, A.
;
Olivieri, A.
;
Chiang, C.W.K.
;
Al-Asadi, H.
;
Dey, K.
;
Joseph, T.A.
;
Liu, C.-C.
;
Der Sarkissian, C.
;
Radzevičiūtė, R.
;
Michel, M.
;
Gradoli, M.G.
;
Marongiu, P.
;
Rubino, S.
;
et al.
1999
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7
Settasatian, C.
;
Whitmore, S.
;
Crawford, J.
;
Bilton, R.
;
Cleton-Jansen, A.M.
;
Sutherland, G.
;
Callen, D.
2014
Mitochondrial genome sequencing in mesolithic North East Europe unearths a new sub-clade within the broadly distributed human haplogroup C1
Der Sarkissian, C.
;
Brotherton, P.
;
Balanovsky, O.
;
Templeton, J.
;
Llamas, B.
;
Soubrier, J.
;
Moiseyev, V.
;
Khartanovich, V.
;
Cooper, A.
;
Haak, W.
;
Genographic Consortium,
;
Achilli, A.
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
2018
A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency
Jansen, S.
;
Hoischen, A.
;
Coe, B.
;
Carvill, G.
;
van Esch, H.
;
Bosch, D.
;
Andersen, U.
;
Baker, C.
;
Bauters, M.
;
Bernier, R.
;
van Bon, B.
;
Claahsen-van der Grinten, H.
;
Gecz, J.
;
Gilissen, C.
;
Grillo, L.
;
Hackett, A.
;
Kleefstra, T.
;
Koolen, D.
;
Kvarnung, M.
;
Larsen, M.
;
et al.
1998
Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
Whitmore, S.
;
Settasatian, C.
;
Crawford, J.
;
Lower, K.
;
McCallum, B.
;
Seshadri, R.
;
Cornelisse, C.
;
Moerland, E.
;
Cleton-Jansen, A.M.
;
Tipping, A.
;
Mathew, C.
;
Savnio, M.
;
Savoia, A.
;
Verlander, P.
;
Auerbach, A.
;
Van Berkel, C.
;
Pronk, J.
;
Doggett, N.
;
Callen, D.
Discover
Author
4
et al.
3
Callen, D.
2
Cleton-Jansen, A.M.
2
Crawford, J.
2
Der Sarkissian, C.
2
Doggett, N.
2
Llamas, B.
2
Settasatian, C.
2
Whitmore, S.
1
Achilli, A.
.
next >
Subject
3
DNA, Complementary
3
Introns
2
Adolescent
2
Adult
2
Child
2
DNA, Mitochondrial
2
Genes
2
Genetics, Population
2
Genome, Human
2
Intellectual Disability
.
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Date issued
5
2010 - 2020
6
1997 - 1999