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

Sally H. Cross

MRC Human Genetics Unit

Institute of Genetics and Molecular Medicine

Edinburgh

UK

[email]@hgu.mrc.ac.uk

Name/email consistency: high

 
 
 
 
 
 
 

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

  1. 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]
  2. 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]
  3. 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]
  4. Isolation of CpG islands from large genomic clones. Cross, S.H., Clark, V.H., Bird, A.P. Nucleic Acids Res. (1999) [Pubmed]
 
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