FOXE3 mutations: genotype‐phenotype correlations
Plaisancié, J., Ragge, N.K., Dollfus, H., Kaplan, J., Lehalle, D., Francannet, C., Morin, G., Colineaux, H., Calvas, P., Chassaing, N.
Published in Clinical genetics (01.04.2018)
Published in Clinical genetics (01.04.2018)
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Presymptomatic diagnosis of neurofibromatosis 2 using linked genetic markers, neuroimaging, and ocular examinations
Baser, M E, Mautner, V F, Ragge, N K, Nechiporuk, A, Riccardi, V M, Klein, J, Sainz, J, Pulst, S M
Published in Neurology (01.11.1996)
Published in Neurology (01.11.1996)
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