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Results: 1-6 |
Results: 6

Authors: Murgia, A Martella, M Polli, R Piermarocchi, S Lo Giudice, G Opocher, G
Citation: A. Murgia et al., Molecular diagnosis of von Hippel-Lindau disease, CONTR NEPHR, 136, 2001, pp. 263-270

Authors: Piermarocchi, S Lo Giudice, G Pilotto, E Bertoja, E Scaroni, C Martella, M Opocher, G Murgia, A
Citation: S. Piermarocchi et al., Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease, GR ARCH CL, 238(7), 2000, pp. 615-620

Authors: Orzan, E Polli, R Martella, M Vinanzi, C Leonardi, M Murgia, A
Citation: E. Orzan et al., Molecular genetics applied to clinical practice: the Cx26 hearing impairment, BR J AUDIOL, 33(5), 1999, pp. 291-295

Authors: Murgia, A Orzan, E Polli, R Martella, M Vinanzi, C Leonardi, E Arslan, E Zacchello, F
Citation: A. Murgia et al., Cx26 deafness: mutation analysis and clinical variability, J MED GENET, 36(11), 1999, pp. 829-832

Authors: Murgia, A Polli, R Martella, M Vinanzi, C Opocher, G
Citation: A. Murgia et al., Molecular diagnosis of inherited diseases (vol 280, pg 73, 1999), CLIN CHIM A, 282(1-2), 1999, pp. 229-229

Authors: Murigia, A Polli, R Martella, M Vinanzi, C Opocher, G
Citation: A. Murigia et al., Molecular diagnosis of inherited diseases, CLIN CHIM A, 280(1-2), 1999, pp. 73-80
Risultati: 1-6 |