C. Bernardo

发表

Mutation analysis of the RPGR gene reveals novel mutations in south European patients with X-linked retinitis pigmentosa

A. Ciccodicola, M. D'urso, M. Mangino, 1999, European Journal of Human Genetics.

Autosomal-dominant Retinitis Pigrnentosa Associated with an Arg-135-Trp Point Mutation of the Rhodopsin Gene

L. Flagiello, E. Vingolo, M. Pannarale, 1996 .

Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening

M. Castori, P. Grammatico, C. Catricalà, 2012, Familial Cancer.

Complex multipathways alterations and oxidative stress are associated with Hailey–Hailey disease

I. Screpanti, D. Taruscio, S. Cialfi, 2010, The British journal of dermatology.

The controversial role of variants in HAMP , BMP 2 , FTL and SLC 40 A 1 genes

F. Torricelli, P. Grammatico, D. Giannarelli, 2015 .

Novel and recurrent p14ARF mutations in Italian familial melanoma

M. Castori, P. Grammatico, C. Catricalà, 2010, Clinical genetics.

Analysis of the miR-34a locus in 62 patients with familial cutaneous melanoma negative for CDKN2A/CDK4 screening

M. Castori, P. Grammatico, C. Catricalà, 2011, Familial Cancer.

Correlation between antioxidants and phototypes in melanocytes cultures. A possible link of physiologic and pathologic relevance.

M. Picardo, P. Grammatico, L. Eibenschutz, 1999, The Journal of investigative dermatology.

A novel germline mutation in CDK4 codon 24 associated to familial melanoma

I. Bottillo, A. Paiardini, S. Bargiacchi, 2018, Clinical genetics.