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Mostrati risultati da 1 a 3 di 3
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
2013-08-05 M. Calvello, S. Tabano, P. Colapietro, S. Maitz, A. Pansa, C. Augello, F. Lalatta, B. Gentilin, F. Spreafico, L. Calzari, D. Perotti, L. Larizza, S. Russo, A. Selicorni, S.M. Sirchia, M. Miozzo
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men
2014-12-01 A. Pansa, S.M. Sirchia, S. Melis, D. Giacchetta, M. Castiglioni, P. Colapietro, S. Fiori, R. Falcone, L. Paganini, E. Bonaparte, G. Colpi, M. Miozzo, S. Tabano
Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro-deletion involving CNTNAP5
2020-01-01 S. Aleo, D. Milani, A. Pansa, P. Marchisio, S. Guerneri, R. Silipigni
Titolo | Data di pubblicazione | Autore(i) | Tipo | File | Abstract |
---|---|---|---|---|---|
Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome | 5-ago-2013 | M. CalvelloS. TabanoP. ColapietroS. MaitzPANSA, ALESSANDRAC. AugelloB. GentilinL. LarizzaS.M. SirchiaM. Miozzo + | Article (author) | - | |
ESX1 mRNA expression in seminal fluid is an indicator of residual spermatogenesis in non-obstructive azoospermic men | 1-dic-2014 | A. PansaS.M. SirchiaS. MelisP. ColapietroS. FioriR. FalconeL. PaganiniE. BonaparteM. MiozzoS. Tabano + | Article (author) | - | |
Autism spectrum disorder and intellectual disability in an inherited 2q14.3 micro-deletion involving CNTNAP5 | 1-gen-2020 | Milani D.Pansa A.Marchisio P.Silipigni R. + | Article (author) | - |
Mostrati risultati da 1 a 3 di 3
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