APA

Grasso M., Faravelli F., Lo Nigro C., Chiurazzi P., Sperandeo M. P., Argusti A., Pomponi M. G., Lecora M., Sebastio G. F., Perroni L., Andria G., Neri G. & Bricarelli F. D. (20000517). Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients. : American journal of medical genetics.

Chicago

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo M P, Argusti A, Pomponi M G, Lecora M, Sebastio G F, Perroni L, Andria G, Neri G and Bricarelli F D. 20000517. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients. : American journal of medical genetics.

Harvard

Grasso M., Faravelli F., Lo Nigro C., Chiurazzi P., Sperandeo M. P., Argusti A., Pomponi M. G., Lecora M., Sebastio G. F., Perroni L., Andria G., Neri G. and Bricarelli F. D. (20000517). Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients. : American journal of medical genetics.

MLA

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo M P, Argusti A, Pomponi M G, Lecora M, Sebastio G F, Perroni L, Andria G, Neri G and Bricarelli F D. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients. : American journal of medical genetics. 20000517.