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

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H.S. Scott

Department of Genetics and Microbiology

University of Geneva Medical School

Switzerland

[email]@*.unige.ch

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Affiliation

Department of Genetics and Microbiology, University of Geneva Medical School, Switzerland. 1998 - 2000

References

Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3. Scott, H.S., Antonarakis, S.E., Mittaz, L., Lalioti, M.D., Younus, F., Mohyuddin, A., Mehdi, S.Q., Gal, A. Adv. Otorhinolaryngol. (2000) [Pubmed]
Characterization of a novel gene, C21orf2, on human chromosome 21q22.3 and its exclusion as the APECED gene by mutation analysis. Scott, H.S., Kyriakou, D.S., Peterson, P., Heino, M., Tähtinen, M., Krohn, K., Chen, H., Rossier, C., Lalioti, M.D., Antonarakis, S.E. Genomics (1998) [Pubmed]
Common mutations in autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients of different origins. Scott, H.S., Heino, M., Peterson, P., Mittaz, L., Lalioti, M.D., Betterle, C., Cohen, A., Seri, M., Lerone, M., Romeo, G., Collin, P., Salo, M., Metcalfe, R., Weetman, A., Papasavvas, M.P., Rossier, C., Nagamine, K., Kudoh, J., Shimizu, N., Krohn, K.J., Antonarakis, S.E. Mol. Endocrinol. (1998) [Pubmed]