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Human Genetics|July 1, 1991
Genotype-phenotype correlation and germline mosaicism in DMD/BMD patients with deletions of the dystrophin geneA E Covone, M Lerone, G RomeoAmerican Journal of Medical Genetics|November 1, 1993
Uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly: report of a new patient with additional findingsM Silengo, M Lerone, G Romeo, et al.American Journal of Medical Genetics|December 1, 1992
Congenital diaphragmatic hernia associated with ipsilateral upper limb reduction defects: report of a case with thumb hypoplasiaM Lerone, M Soliani, D Corea, et al.Pediatric Radiology|January 1, 1990
A new syndrome with cerebro-oculo-skeletal-renal involvementM C Silengo, M Lerone, A Pelizza, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1990
[Lip pits and Van der Woude syndrome. Description of a new familial case]A Rizzo, M Lerone, G Martucciello, et al.American Journal of Medical Genetics|January 24, 1998
Ectodermal abnormalities in Kabuki syndromeM Lerone, M Priolo, A Naselli, et al.Journal of Pediatric Surgery|September 11, 2004
Currarino syndrome: proposal of a diagnostic and therapeutic protocolG Martucciello, M Torre, E Belloni, et al.Clinical Genetics|February 1, 1992
Oculocerebral syndrome with hypopigmentation (Cross syndrome): report of a new caseM Lerone, A Pessagno, A Taccone, et al.Journal of Medical Genetics|March 21, 1998
Ectodermal dysplasia, primary hypothyroidism, and agenesis of the corpus callosum: variable expression of a single syndrome?M Silengo, L Silvestro, G Capizzi, et al.Human Genetics|April 1, 1991
Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutationsN Archidiacono, M Lerone, M Rocchi, et al.Pageof 97