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Lovicu, FJ, Kolle, G, Yamada, T, Little, MH, McAvoy, JW.
Expression of Crim1 during murine ocular development.
Cells and Development
94(1-2)
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261 -265
2000
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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.
Human Mutation
15(4)
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389 -389
2000
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Hargrave, M, James, K, Nield, K, Toomes, C, Georgas, K, Sullivan, T, Verzijl, HTFM, 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.
Human Genetics
106(4)
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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.
Circulation Research
86(2)
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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.
Cells and Development
90(2)
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181 -193
2000
view publication