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Human Genetics|July 1, 1986
Ring chromosome 21 in healthy persons: different consequences in females and in malesB Dallapiccola, V De Filippis, A Notarangelo, et al.American Journal of Medical Genetics|November 1, 1990
Jeune syndrome associated with cystinuria: report of two sistersS Rinaldi, C Dionisi-Vici, B Goffredo, et al.Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Congenital heart defects in patients with DiGeorge/velocardiofacial syndrome and del22q11B Marino, M C Digilio, A Toscano, et al.American Journal of Medical Genetics|March 1, 1992
New case of Bartsocas-Papas syndrome surviving at 20 monthsA Giannotti, M C Digilio, L Standoli, et al.The Journal of Pediatrics|December 10, 1999
Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canalB Marino, M C Digilio, A Toscano, et al.American Journal of Medical Genetics|February 7, 1998
Intrafamilial variability of Pfeiffer-type cardiocranial syndromeM C Digilio, B Marino, U Borzaga, et al.Journal of the American Aging Association|April 23, 2013
TCR Vβ repertoire in an Italian longeval population including centenariansG Pennesi, M Morellini, P Lulli, et al.Human Pathology|March 1, 1991
Rapid perinatal growth mimicking malignant transformation in a giant congenital melanocytic nevusD Angelucci, P G Natali, P L Amerio, et al.European Journal of Human Genetics : EJHG|October 20, 2000
Fine mapping of a distinctive autosomal dominant vacuolar neuromyopathy using 11 novel microsatellite markers from chromosome band 19p13.3F Sangiuolo, E Bruscia, F Capon, et al.Cell Biochemistry and Function|June 24, 1998
Genomic instability associated with myotonic dystrophy does not involve p53 expression and activityM Gennarelli, M Lucarelli, P Amicucci, et al.Pageof 38