Items where Author is "Haan, E"

SPURLOCK, G., BENNETT, E., CHUZHANOVA, N., THOMAS, N., HOI-PING, J., SIDE, L., DAVIES, S., HAAN, E., KERR, K., HUSON, S.M. and UPADHYAYA, M., 2009. SPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the NF1 phenotype. Journal of Medical Genetics, 46, pp. 431-437.

UPADHYAYA, M., HUSON, S.M., DAVIES, M., THOMAS, N., CHUZHANOVA, N., GIOVANNINI, S., EVANS, D.G., 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.