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American Journal of Medical Genetics|September 15, 1991
Hypomelanosis of Ito associated with chromosomal translocation involving Xp11M S Lungarotti, C Martello, A Calabro, et al.American Journal of Medical Genetics|July 15, 1994
X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second familyM S Lungarotti, C Martello, G Barboni, et al.Helvetica Paediatrica Acta|August 1, 1976
Treatment of acrodermatitis enteropathica with zinc sulphate. Rerport of 3 casesM S Lungarotti, S Rufini, A Calabro, et al.American Journal of Medical Genetics|June 1, 1987
Multiple congenital anomalies associated with apparently normal maternal intake of vitamin A: a phenocopy of the isotretinoin syndrome?M S Lungarotti, D Marinelli, T Mariani, et al.Journal of Medical Genetics|October 1, 1980
De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomicsM S Lungarotti, A Falorni, A Calabro, et al.American Journal of Medical Genetics|July 1, 1991
Acrocallosal syndrome: a new caseM S Lungarotti, D Marinelli, D Mezzetti, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|January 1, 1980
Chromosome 13 deletion syndrome: report of a new case and discussion of the different etiologic patterns of retinoblastomaM S Lungarotti, G Mariotti, C Quarta, et al.La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1992
[Spondylo-costal dysostosis: presentation of a new case with autosomal dominant heredity and discussion of problems in genetic counseling]C Martello, G Stangoni, D Mezzetti, et al.Human Genetics|January 1, 1979
Interstitial deletion 13q syndromes: a report on two unrelated patientsM Serena-Lungarotti, A Calabro, G Mariotti, et al.Pediatric Radiology|January 1, 1993
Lethal short rib syndrome of the Beemer type without polydactylyM S Lungarotti, C Martello, I Marinelli, et al.Pageof 14