Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rate: Molecular Genetics and Genomic Medicine

I. Catusi, M.P. Recalcati, I. Bestetti, M. Garzo, C. Valtorta, M. Alfonsi, A. Alghisi, S. Cappellani, R. Casalone, R. Caselli, C. Ceccarini, C. Ceglia, A.M. Ciaschini, D. Coviello, F. Crosti, A. D'Aprile, A. Fabretto, R. Genesio, M. Giagnacovo, P. GranataI. Longo, M. Malacarne, G. Marseglia, A. Montaldi, A.M. Nardone, C. Palka, V. Pecile, C. Pessina, D. Postorivo, S. Redaelli, A. Renieri, C. Rigon, F. Tiberi, M. Tonelli, N. Villa, A. Zilio, D. Zuccarello, A. Novelli, L. Larizza, D. Giardino

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