Hasil Pencarian - A. Percesepe

  • Menampilkan 1 - 3 hasil dari 3
Perbaiki Hasil
  1. 1
    A mild phenotype of sensorineural hearing loss and palmoplantar keratoderma caused by a novel GJB2 dominant mutation

    A mild phenotype of sensorineural hearing loss and palmoplantar keratoderma caused by a novel GJB2 dominant mutation oleh I. Stanghellini, E. Genovese, S. Palma, C. Falcinelli, L. Presutti, A. Percesepe

    Diterbitkan 2017-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever

    A new MEFV gene mutation in an Iranian patient with familial Mediterranean fever oleh S. Farjadian, F. Bonatti, A. Soriano, M. Reina, A. Adorni, C. Graziano, M. Moghtaderi, A. Percesepe, G. Romeo, D. Martorana

    Diterbitkan 2019-07-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    ItaLynch: an ongoing Italian study to evaluate the feasibility of mainstreaming the diagnosis of Lynch syndrome in colorectal cancer patients

    ItaLynch: an ongoing Italian study to evaluate the feasibility of mainstreaming the diagnosis of Lynch syndrome in colorectal cancer patients oleh A. Puccini, F. Grillo, M. Fassan, S. Lonardi, M. Genuardi, R. Cannizzaro, G.M. Cavestro, F. Marmorino, V. Conca, L. Salvatore, F. Bergamo, F. Tosi, F. Morano, V. Daprà, C. Molica, D. Barana, A. Guglielmi, C. Signorelli, M. D’Amico, F. Zoratto, D. Iacono, A. Morabito, G. Martini, A. Fabbroncini, M. Duro, G. Bruera, A. Auriemma, B. Bonanni, A. Percesepe, M. Dono, L. Battistuzzi, R. Labianca, L. Boni, S. Sciallero

    Diterbitkan 2024-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: