Items where Author is "Messiaen, L"

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Journal article

Zickler, AM, Hampp, S, Messiaen, L, Bengesser, K, Mussotter, T, Roehl, AC, Wimmer, K, Mautner, V, Kluwe, L, Upadhyaya, M, Pasmant, E, Chuzhanova, N ORCID: 0000-0002-4655-3618, Kestler, HA, Högel, J, Legius, E, Claes, K, Cooper, DN and Kehrer-Sawatzki, H, 2012. Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions. Human Mutation, 33, pp. 372-383.

Vogt, J, Mussotter, T, Bengesser, K, Claes, K, Högel, J, Chuzhanova, N ORCID: 0000-0002-4655-3618, Fu, C, Van den Ende, J, Mautner, VF, Cooper, DN, Messiaen, L and Kehrer-Sawatzki, H, 2012. Identification of recurrent type-2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder. Human Mutation, 33 (11), pp. 1599-1609.

Upadhyaya, M, Huson, SM, Davies, M, Thomas, N, Chuzhanova, N ORCID: 0000-0002-4655-3618, Giovannini, S, Evans, DG, Howard, E, Kerr, B, Griffiths, S, Consoli, C, Side, L, Adams, D, Pierpoint, M, Hachen, R, Barnicoat, A, Li, H, Wallace, P, Stevenson, D, Viskochil, D, Baralle, D, Haan, E, Turnpenny, P, Riccardi, V, Lazaro, C and Messiaen, L, 2007. An absence of cutaneous neurofibromas associated with a 3-bp in-frame deletion in exon 17 of the NF1 gene (c.2970_2972 delAAT): Evidence of a clinically significant NF1 genotype-phenotype correlation. American Journal of Human Genetics, 80, pp. 140-151.

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