M. Fava

Incidence of RET mutations in patients with Hirschsprung's disease.

P. Tam, R. Hofstra, I. Ceccherini, 2000, Journal of pediatric surgery.

Functional characterization of a minimal sequence essential for the expression of human TLX2 gene.

R. Ravazzolo, I. Ceccherini, T. Bachetti, 2009, BMB reports.

Assignment1 of the HOX11L2 gene to human chromosome band 5q35.1 and of its murine homolog to mouse chromosome bands 11A4–A5 by in situ hybridization

R. Ravazzolo, I. Ceccherini, I. Matera, 2001, Cytogenetic and Genome Research.

The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cells.

R. Ravazzolo, D. Fornasari, I. Ceccherini, 2006, The Biochemical journal.

Evaluation of the HOX11L1 gene as a candidate for congenital disorders of intestinal innervation

R. Cusano, G. Romeo, I. Ceccherini, 2000, Journal of medical genetics.

HOX11L1: a promoter study to evaluate possible expression defects in intestinal motility disorders.

R. Ravazzolo, R. De Giorgio, R. Cusano, 2002, International journal of molecular medicine.