20182019

Research output per year

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Fingerprint Dive into the research topics where Luciano Calzari is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation

Demond, H., Anvar, Z., Jahromi, B. N., Sparago, A., Verma, A., Davari, M., Calzari, L., Russo, S., Jahromi, M. A., Monk, D., Andrews, S., Riccio, A. & Kelsey, G., Dec 17 2019, In : Genome Medicine. 11, 1, 84.

Research output: Contribution to journalArticle

Open Access
  • Discrepant molecular and clinical diagnoses in Beckwith-Wiedemann and Silver-Russell syndromes

    Mackay, D. J. G., Bliek, J., Lombardi, M. P., Russo, S., Calzari, L., Guzzetti, S., Izzi, C., Selicorni, A., Melis, D., Temple, K., Maher, E., Brioude, F., Netchine, I. & Eggermann, T., Mar 4 2019, In : Genetical Research. 101, p. e3

    Research output: Contribution to journalArticle

  • Open Access
  • Molecular Etiology Disclosed by Array CGH in Patients With Silver–Russell Syndrome or Similar Phenotypes

    Crippa, M., Bonati, M. T., Calzari, L., Picinelli, C., Gervasini, C., Sironi, A., Bestetti, I., Guzzetti, S., Bellone, S., Selicorni, A., Mussa, A., Riccio, A., Ferrero, G. B., Russo, S., Larizza, L. & Finelli, P., Oct 15 2019, In : Frontiers in Genetics. 10, 955.

    Research output: Contribution to journalArticle

    Open Access