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Clinical features and follow-up in patients with 22q11.2 deletion syndrome. [1]

TitoloClinical features and follow-up in patients with 22q11.2 deletion syndrome.
Publication TypeJournal Article
AuthorsCancrini, C [2], Puliafito, P [3], Digilio, MCristina [4], Soresina, A [5], Martino, S [6], Rondelli, R [7], Consolini, R [8], Ruga, EMaria [9], Cardinale, F [10], Finocchi, A [11], Romiti, MLuisa [12], Martire, B [13], Bacchetta, R [14], Albano, V [15], Carotti, A [16], Specchia, F [17], Montin, D [18], Cirillo, E [19], Cocchi, G [20], Trizzino, A [21], Bossi, G [22], Milanesi, O [23], Azzari, C [24], Corsello, G [25], Pignata, C [26], Aiuti, A [27], Pietrogrande, MCristina [28], Marino, B [29], Ugazio, AGiovanni [30], Plebani, A [31], Rossi, P [32]
Corporate AuthorsItalian Network for Primary Immunodeficiencies [33]
PubMed ID24657119 [34]

Source URL: https://www.burlo.trieste.it/ricerca/pubblicazioni/clinical-features-and-follow-patients-22q112-deletion-syndrome#comment-0

Collegamenti
[1] https://www.burlo.trieste.it/ricerca/pubblicazioni/clinical-features-and-follow-patients-22q112-deletion-syndrome
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[34] http://www.ncbi.nlm.nih.gov/pubmed/24657119?dopt=Abstract