S. Lo Cicero

Theratyping cystic fibrosis in vitro in ALI culture and organoid models generated from patient-derived nasal epithelial conditionally reprogrammed stem cells

M. Biffoni, M. Falchi, G. Cimino, 2021, European Respiratory Journal.

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle

B. Dallapiccola, G. Novelli, F. Sangiuolo, 1992, Cell biochemistry and function.

SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females.

Meghan C Towne, Carol J. Saunders, B. V. van Bon, 2021, American journal of human genetics.

A tool for the molecular analysis of an early lethal disease: slide-PCR in spinal muscular atrophy patients.

B. Dallapiccola, G. Novelli, F. Capon, 1993, Molecular and Cellular Probes.