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

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Simon T. Holden

Department of Clinical Genetics

Guy's Hospital

London

[email]@gstt.nhs.uk

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Affiliations

Department of Clinical Genetics, Guy's Hospital, London, UK. 2010
Department of Clinical Genetics, 7th Floor New Guy's House, Guy's Hospital, St Thomas Street, UK. 2006

References

A de novo duplication of Xp11.22-p11.4 in a girl with intellectual disability, structural brain anomalies, and preferential inactivation of the normal X chromosome. Holden, S.T., Clarkson, A., Thomas, N.S., Abbott, K., James, M.R., Willatt, L. Am. J. Med. Genet. A (2010) [Pubmed]
Fanconi anaemia complementation group B presenting as X linked VACTERL with hydrocephalus syndrome. Holden, S.T., Cox, J.J., Kesterton, I., Thomas, N.S., Carr, C., Woods, C.G. J. Med. Genet. (2006) [Pubmed]