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Results 1-10 of 17 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
1996
The stoned locus of drosophila melanogaster produces a dicistronic transcript and encodes two distinct polypeptides
Andrews, J.
;
Smith, M.
;
Merakovsky, J.
;
Coulson, M.
;
Hannan, F.
;
Kelly, L.
2007
Kit signaling is essential for development and maintenance of interstitial cells of Cajal and electrical rhythmicity in the embryonic gastrointestinal tract
Spencer, E.
;
Ro, S.
;
Bayguinov, Y.
;
Sanders, K.
;
Ward, S.
2005
Identification and characterization of avihepadnaviruses isolated from exotic anseriformes maintained in captivity
Guo, H.
;
Mason, W.
;
Aldrich, C.
;
Saputelli, J.
;
Miller, D.
;
Jilbert, A.
;
Newbold, 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.
2010
A focal Eeilepsy and intellectual disability syndrome is due to a mutation in TBC1D24
Bahlo, M.
;
Jolly, L.
;
Afawi, Z.
;
Gardner, A.
;
Oliver, K.
;
Tan, S.
;
Coffey, A.
;
Mulley, J.
;
Dibbens, L.
;
Simri, W.
;
Shalata, A.
;
Kivity, S.
;
Jackson, G.
;
Berkovic, S.
;
Gecz, J.
;
Corbett, M.
2009
Identifying candidate serum biomarkers of exposure to tunicamycins in rats using two-dimensional electrophoresis
Penno, M.
;
Bacic, A.
;
Colegate, S.
;
Hoffmann, P.
;
Michalski, W.
2013
A heterozygous moth genome provides insights into herbivory and detoxification
You, M.
;
Baxter, S.
2001
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy
Phillips, H.
;
Favre, I.
;
Kirkpatrick, M.
;
Zuberi, S.
;
Goudie, D.
;
Heron, S.
;
Scheffer, I.
;
Sutherland, G.
;
Berkovic, S.
;
Bertrand, D.
;
Mulley, J.
2007
DMRT gene cluster analysis in the platypus: New insights into genomic organization and regulatory regions
El-Mogharbel, N.
;
Wakefield, M.
;
Deakin, J.
;
Tsend-Ayush, E.
;
Grutzner, F.
;
Alsop, A.
;
Ezaz, T.
;
Graves, J.
2002
Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome
Lower, K.
;
Turner, G.
;
Kerr, B.
;
Mathews, K.
;
Shaw, M.
;
Gedeon, A.
;
Schelley, S.
;
Hoyme, H.
;
White, S.
;
Delatycki, M.
;
Lampe, A.
;
Clayton-Smith, J.
;
Stewart, H.
;
van Ravenswaay, C.
;
de Vries, B.
;
Cox, B.
;
Grompe, M.
;
Ross, S.
;
Thomas, P.
;
Mulley, J.
;
et al.
Discover
Author
6
Mulley, J.
3
Baxter, S.
3
Berkovic, S.
3
Scheffer, I.
3
Sutherland, G.
2
El-Mogharbel, N.
2
Gecz, J.
2
Gedeon, A.
2
Graves, J.
2
Grutzner, F.
.
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Subject
10
Amino Acid Sequence
9
Humans
7
Base Sequence
7
Mutation
6
Mice
6
Pedigree
5
Evolution, Molecular
5
X Chromosome
4
Intellectual Disability
4
Sequence Analysis, DNA
.
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Date issued
3
2010 - 2013
11
2000 - 2009
3
1996 - 1999