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Clinical Genetics|September 1, 1994
Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotypeM C Digilio, R Mingarelli, B Marino, et al.British Journal of Audiology|July 13, 2000
Audiological findings in patients with microdeletion 22q11 (di George/velocardiofacial syndrome)M C Digilio, C Pacifico, L Tieri, et al.American Journal of Medical Genetics|May 26, 1999
Cardiac malformations in patients with oral-facial-skeletal syndromes: clinical similarities with heterotaxiaM C Digilio, B Marino, A Ammirati, et al.Archives of Pediatrics & Adolescent Medicine|April 18, 2000
Clinical and cardiorespiratory assessment in children with Down syndrome without congenital heart diseaseE Pastore, B Marino, A Calzolari, et al.American Journal of Medical Genetics|November 7, 1998
Congenital heart defect in sibs with discordant karyotypesM C Digilio, B Marino, S A Canepa, et al.Journal of Medical Genetics|December 10, 1997
Radial aplasia and chromosome 22q11 deletionM C Digilio, A Giannotti, B Marino, et al.American Journal of Diseases of Children (1960)|December 1, 1993
Risk of congenital heart defects in relatives of patients with atrioventricular canalM C Digilio, B Marino, M P Cicini, et al.The American Journal of Cardiology|March 1, 1996
Associated cardiac anomalies in isolated and syndromic patients with tetralogy of FallotB Marino, M C Digilio, S Grazioli, et al.American Journal of Medical Genetics|November 7, 1998
Noonan syndrome and aortic coarctationM C Digilio, B Marino, F Picchio, et al.Clinical Genetics|April 19, 2003
Spectrum of clinical variability in familial deletion 22q11.2: from full manifestation to extremely mild clinical anomaliesM C Digilio, A Angioni, M De Santis, et al.Pageof 34