Romeo Carrozzo

Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

J. Korenberg, G. Gimelli, M. Digilio, 2000, Circulation.

Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndrome.

D. Ledbetter, S. Christian, P. Simi, 1997, American journal of human genetics.

Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoire.

D. Ledbetter, D. Lancet, H. Lehrach, 1994, Human molecular genetics.

The human ROX gene: genomic structure and mutation analysis in human breast tumors.

D. Ledbetter, A. Reymond, A. Ballabio, 1998, Genomics.