Search Results - Barrano, B

  • Showing 1 - 6 results of 6
Refine Results
  1. 1
    Hereditary haemorrhagic telangiectasia and genetic thrombophilia

    Hereditary haemorrhagic telangiectasia and genetic thrombophilia by Bianca, S, Cutuli, N, Bianca, M, Barrano, B, Cataliotti, A, Barone, C, Indaco, L, Milana, G

    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  2. 2
    Hereditary haemorrhagic telangiectasia and genetic thrombophilia: Letter

    Hereditary haemorrhagic telangiectasia and genetic thrombophilia: Letter by Bianca, S, Cutuli, N, Bianca, M, Barrano, B, Cataliotti, A, Barone, C, Indaco, L, Milana, G

    Get full text
    Article
    Save to List
    Saved in:
  3. 3
    Hyperphenylalaninemia and birth weight

    Hyperphenylalaninemia and birth weight by Bianca, Sebastiano, Meli, Concetta, Barrano, Barbara, Mollica, Florindo

    Published in Annales de génétique
    Get full text
    Items that this one cites
    Article
    Save to List
    Saved in:
  4. 4
    AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

    AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders by Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L., Castori, Marco, Marsh, Sarah E., Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S., Abdel-Aleem, Alice, Abdel-Salam, Ghada M. H., Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P., Dobyns, William B., Krishnamoorthy, Kalpathy S., Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D., Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G.

    Published in Annals of neurology
    Get full text
    Items that this one cites
    Items that cite this one
    Article
    Save to List
    Saved in:
  5. 5
    DMO03 CEP290 mutations are a frequent cause of Joubert syndrome with oculo-renal involvement

    DMO03 CEP290 mutations are a frequent cause of Joubert syndrome with oculo-renal involvement by Valente, E.M, Brancati, F, Barrano, G, Silhavy, J.L, Marsh, S.E, Bertini, E, Boltshauser, E, Dallapiccola, B, Gleeson, J.G

    Get full text
    Article
    Save to List
    Saved in:
  6. 6
    AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders

    AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders by Valente, Enza Maria, Brancati, Francesco, Silhavy, Jennifer L, Castori, Marco, Marsh, Sarah E, Barrano, Giuseppe, Bertini, Enrico, Boltshauser, Eugen, Zaki, Maha S, Abdel-Aleem, Alice, Abdel-Salam, Ghada MH, Bellacchio, Emanuele, Battini, Roberta, Cruse, Robert P, Dobyns, William B, Krishnamoorthy, Kalpathy S, Lagier-Tourenne, Clotilde, Magee, Alex, Pascual-Castroviejo, Ignacio, Salpietro, Carmelo D, Sarco, Dean, Dallapiccola, Bruno, Gleeson, Joseph G

    Published in Annals of neurology
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: