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Results: 5
Molecular diagnosis of von Hippel-Lindau disease
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
Molecular genetics applied to clinical practice: the Cx26 hearing impairment
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
Cx26 deafness: mutation analysis and clinical variability
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
Molecular diagnosis of inherited diseases (vol 280, pg 73, 1999)
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
Molecular diagnosis of inherited diseases
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
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