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Results:
1-7
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Results: 7
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:
Bisogno, G
Murgia, A
Mammi, I
Strafella, MS
Carli, M
Citation: G. Bisogno et al., Rhabdomyosarcoma in a patient with cardio-facio-cutaneous syndrome, J PED H ONC, 21(5), 1999, pp. 424-427
Authors:
Perilongo, G
Moras, P
Carollo, C
Battistella, A
Clementi, M
Laverda, A
Murgia, A
Citation: G. Perilongo et al., Spontaneous partial regression of low-grade glioma in children with neurofibromatosis-1: A real possibility, J CHILD NEU, 14(6), 1999, pp. 352-356
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
Risultati:
1-7
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