APA

Fontana L., Bedeschi M. F., Maitz S., Cereda A., Faré C., Motta S., Seresini A., D'Ursi P., Orro A., Pecile V., Calvello M., Selicorni A., Lalatta F., Milani D., Sirchia S. M., Miozzo M. & Tabano S. (20190306). Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. : Epigenetics.

Chicago

Fontana L, Bedeschi M F, Maitz S, Cereda A, Faré C, Motta S, Seresini A, D'Ursi P, Orro A, Pecile V, Calvello M, Selicorni A, Lalatta F, Milani D, Sirchia S M, Miozzo M and Tabano S. 20190306. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. : Epigenetics.

Harvard

Fontana L., Bedeschi M. F., Maitz S., Cereda A., Faré C., Motta S., Seresini A., D'Ursi P., Orro A., Pecile V., Calvello M., Selicorni A., Lalatta F., Milani D., Sirchia S. M., Miozzo M. and Tabano S. (20190306). Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. : Epigenetics.

MLA

Fontana L, Bedeschi M F, Maitz S, Cereda A, Faré C, Motta S, Seresini A, D'Ursi P, Orro A, Pecile V, Calvello M, Selicorni A, Lalatta F, Milani D, Sirchia S M, Miozzo M and Tabano S. Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders. : Epigenetics. 20190306.