Giuseppe Novelli

Mapping a dominant form of multinodular goiter to chromosome Xp22.

B. Dallapiccola, S. Filetti, G. Novelli, 2000, American journal of human genetics.

A serine-to-arginine (AGT-to-CGT) mutation in codon 549 of the CFTR gene in an Italian patient with severe cystic fibrosis.

B. Dallapiccola, G. Novelli, F. Sangiuolo, 1991, Genomics.

In vitro correction of cystic fibrosis epithelial cell lines by small fragment homologous replacement (SFHR) technique

F. Sangiuolo, A. Nardone, E. Bonifazi, 2002, BMC Medical Genetics.

Targeted correction of a defective selectable marker gene in human epithelial cells by small DNA fragments.

B. Dallapiccola, G. Novelli, A. Colosimo, 2001, Molecular therapy : the journal of the American Society of Gene Therapy.

Expression analysis and protein localization of the human HPC-1/syntaxin 1A, a gene deleted in Williams syndrome.

B. Dallapiccola, G. Novelli, F. Sangiuolo, 1999, Genomics.

Assignment of the slow troponin T (TNNT1) gene to chromosome 19 using polymerase chain reaction

Massimo Gennarelli, Mariano Rocchi, Giuseppe Novelli, 1992, Human Genetics.

Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma.

B. Dallapiccola, G. Novelli, M. Gennarelli, 2000, Clinical chemistry.

Male Hypogonadism in Myotonic Dystrophy is Related to (Ctg)N Triplet Mutation

C. Angelini, B. Dallapiccola, G. Novelli, 1994, Journal of endocrinological investigation.