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
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 11-20 of 23 (Search time: 0.002 seconds).
previous
1
2
3
next
Item hits:
Preview
Issue Date
Title
Author(s)
1997
Ancient missense mutations in a new member of the RoRet gene family are likely to cause Familial Mediterranean Fever
Aksentijevich, I.
;
Centola, M.
;
Deng, Z.
;
Sood, R.
;
Balow, J.
;
Wood, G.
;
Zaks, N.
;
Mansfield, E.
;
Chen, X.
;
Eisenberg, S.
;
Vedula, A.
;
Shafran, N.
;
Raben, N.
;
Pras, E.
;
Pras, M.
;
Kastner, D.
;
Blake, T.
;
Baxevanis, A.
;
Robbins, C.
;
Krizman, D.
;
et al.
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.
1997
Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2
Horwitz, M.
;
Benson, K.
;
Li, F.Q.
;
Wolff, J.
;
Leppert, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Yu, S.
;
Hewett, D.
;
Richards, R.
;
Raskind, W.
1996
A novel X-linked gene, G4.5. is responsible for Barth Syndrome
Bione, S.
;
D'Adamo, P.
;
Maestrini, E.
;
Gedeon, A.
;
Bolhuis, P.
;
Toniolo, D.
1998
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
Cavanaugh, J.
;
Callen, D.
;
Wilson, S.
;
Stanford, P.
;
Sraml, M.
;
Gorska, M.
;
Crawford, J.
;
Whitmore, S.
;
Shlegel, C.
;
Foote, S.
;
Kohonen-Corish, M.
;
Pavli, P.
1997
Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13
Nomiyama, H.
;
Imai, T.
;
Kusuda, J.
;
Miura, R.
;
Callen, D.
;
Yoshie, O.
1998
Localisation of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.
Kremmidiotis, G.
;
Baker, E.
;
Crawford, J.
;
Eyre, H.
;
Nahmias, J.
;
Callen, D.
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.
1999
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation
Gecz, J.
;
Barnett, S.
;
Liu, J.
;
Hollway, G.
;
Donnelly, A.
;
Eyre, H.
;
Eshkevari, H.
;
Baltazar, R.
;
Grunn, A.
;
Nagaraja, R.
;
Gilliam, C.
;
Peltonen, L.
;
Sutherland, G.
;
Baron, M.
;
Mulley, J.
1998
ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, & is shown to be expressed in primitive hematopoietic precursors.
Kuss, B.
;
O'Neill, G.
;
Eyre, H.
;
Doggett, N.
;
Callen, D.
;
Davey, R.
Discover
Author
9
Mulley, J.
7
Callen, D.
5
Eyre, H.
5
Gedeon, A.
3
Donnelly, A.
3
Sutherland, G.
2
Aksentijevich, I.
2
Baker, E.
2
Blake, T.
2
Centola, M.
.
next >
Subject
23
Humans
17
Male
13
Female
9
Chromosomes, Human, Pair 16
9
Genetic Linkage
8
Genetic Markers
8
X Chromosome
7
Molecular Sequence Data
6
Intellectual Disability
6
Pedigree
.
next >
Date issued
1
2010 - 2017
22
1996 - 1999