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Little, M, Carman, G, Donaldson, E.
Novel WT1 exon 9 mutation (D396Y) in a patient with early onset Denys Drash syndrome..
Hum Mutat
15(4)
:
389
2000
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Hargrave, M, James, K, Nield, K, Toomes, C, Georgas, K, Sullivan, T, Verzijl, HT, Oley, CA, Little, M, De Jonghe, P, et al.
Fine mapping of the neurally expressed gene SOX14 to human 3q23, relative to three congenital diseases..
Hum Genet
106(4)
:
432 -439
2000
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Bellomo, D, Headrick, JP, Silins, GU, Paterson, CA, Thomas, PS, Gartside, M, Mould, A, Cahill, MM, Tonks, ID, Grimmond, SM, et al.
Mice lacking the vascular endothelial growth factor-B gene (Vegfb) have smaller hearts, dysfunctional coronary vasculature, and impaired recovery from cardiac ischemia..
Circ Res
86(2)
:
E29 -E35
2000
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Kolle, G, Georgas, K, Holmes, GP, Little, MH, Yamada, T.
CRIM1, a novel gene encoding a cysteine-rich repeat protein, is developmentally regulated and implicated in vertebrate CNS development and organogenesis..
Mech Dev
90(2)
:
181 -193
2000
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Passey, RJ, Williams, E, Lichanska, AM, Wells, C, Hu, S, Geczy, CL, Little, MH, Hume, DA.
A null mutation in the inflammation-associated S100 protein S100A8 causes early resorption of the mouse embryo..
J Immunol
163(4)
:
2209 -2216
1999
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