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American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.Journal of Medical Genetics|March 2, 1999
Microdeletion 22q11 and oesophageal atresiaM C Digilio, B Marino, P Bagolan, et al.American Journal of Medical Genetics|September 19, 1997
Tricuspid atresia and 22q11 deletionB Marino, M C Digilio, G Novelli, 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.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.American Journal of Medical Genetics|September 20, 2000
Heterotaxy with left atrial isomerism in a patient with deletion 18pM C Digilio, B Marino, A Giannotti, et al.Teratology|April 25, 2000
Familial recurrence of nonsyndromic interrupted aortic arch and truncus arteriosus with atrioventricular canalM C Digilio, B Marino, A M Musolino, et al.The American Journal of Cardiology|June 15, 1996
Comparison of occurrence of genetic syndromes in ventricular septal defect with pulmonic stenosis (classic tetralogy of Fallot) versus ventricular septal defect with pulmonic atresiaM C Digilio, B Marino, S Grazioli, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Auxological evaluation in patients with DiGeorge/velocardiofacial syndrome (deletion 22q11.2 syndrome)M C Digilio, B Marino, M Cappa, et al.Pageof 34