Skip navigation
Home
Browse
Communities
& Collections
Browse Items by:
Issue Date
Author
Title
Advisor
Help
Sign on to:
My DSpace
Receive email
updates
Edit Profile
Adelaide Research & Scholarship
Adelaide Research & Scholarship
Search
Search:
All collections
Schools and Disciplines
School of Molecular and Biomedical Science
Genetics
Genetics publications
for
Current filters:
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Start a new search
Add filters:
Use filters to refine the search results.
Title
Author
Subject
Date Issued
Advisor
School
Department
Organisation
Equals
Contains
ID
Not Equals
Not Contains
Not ID
Results 1-8 of 8 (Search time: 0.002 seconds).
previous
1
next
Item hits:
Preview
Issue Date
Title
Author(s)
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.
1998
Dorsal-mediated repression requires the formation of a multiprotein repression complex at the ventral silencer.
Valentine, S.
;
Chen, G.
;
Shandala, T.
;
Fernandez, J.
;
Mische, S.
;
Saint, R.
;
Courey, A.
1998
Analysis of a Drosophila cyclin E hypomorphic mutation suggests a novel role for Cyclin E in cell proliferation control during eye imaginal disc development.
Secombe, J.
;
Pispa, J.
;
Saint, R.
;
Richardson, H.
1998
Neural precursor differentiation into astrocytes requires signaling through the leukemia inhibitory factor receptor.
Koblar, S.
;
Turnley, A.
;
Classon, B.
;
Reid, K.
;
Ware, C.
;
Cheema, S.
;
Murphy, M.
;
Bartlett, P.
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.
1998
The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogaster
Coulson, M.
;
Robert, S.
;
Eyre, H.
;
Saint, R.
1998
Localisation of the human NMDAR2D receptor subunit gene (GRIN2D) to 19q13.1-qter, the NMDAR2A subunit gene to 16p13.2 (GRIN2A), and the NMDAR2C subunit gene (GRIN2C) to 17q24-q25 using somatic cell hybrid and radiation hybrid mapping panels.
Kalsi, G.
;
Whiting, P.
;
Bourdelles, B.
;
Callen, D.
;
Barnard, E.
;
Gurling, H.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
Discover
Author
4
Saint, R.
2
Eyre, H.
2
Mulley, J.
1
Allen, K.
1
Bagrodia, S.
1
Barnard, E.
1
Bartlett, P.
1
Berkovic, S.
1
Bourdelles, B.
1
Callen, D.
.
next >
Subject
5
Humans
4
Male
4
Mice
4
Molecular Sequence Data
3
Chromosomes, Human, Pair 19
3
DNA-Binding Proteins
3
Drosophila melanogaster
3
Drosophila Proteins
3
Female
3
Pedigree
.
next >