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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Sally H. Cross

MRC Human Genetics Unit

Institute of Genetics and Molecular Medicine

Edinburgh

[email]@hgu.mrc.ac.uk

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Affiliations

MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, Edinburgh, UK. 2011
Comparative and Developmental Genetics Section, MRC Human Genetics Unit, Edinburgh, UK. 2004
Institute of Cell and Molecular Biology, University of Edinburgh, Darwin Building, King's Buildings, UK. 1999 - 2000

References

The Opdc missense mutation of Pax2 has a milder than loss-of-function phenotype. Cross, S.H., McKie, L., West, K., Coghill, E.L., Favor, J., Bhattacharya, S., Brown, S.D., Jackson, I.J. Hum. Mol. Genet. (2011) [Pubmed]
Haploinsufficiency for Phox2b in mice causes dilated pupils and atrophy of the ciliary ganglion: mechanistic insights into human congenital central hypoventilation syndrome. Cross, S.H., Morgan, J.E., Pattyn, A., West, K., McKie, L., Hart, A., Thaung, C., Brunet, J.F., Jackson, I.J. Hum. Mol. Genet. (2004) [Pubmed]
CpG island libraries from human chromosomes 18 and 22: landmarks for novel genes. Cross, S.H., Clark, V.H., Simmen, M.W., Bickmore, W.A., Maroon, H., Langford, C.F., Carter, N.P., Bird, A.P. Mamm. Genome (2000) [Pubmed]
Isolation of CpG islands from large genomic clones. Cross, S.H., Clark, V.H., Bird, A.P. Nucleic Acids Res. (1999) [Pubmed]