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American Journal of Medical Genetics|February 15, 1992
Nonrandom association of atrioventricular canal and del (8p) syndromeB Marino, A Reale, A Giannotti, et al.
Journal of Medical Genetics|March 1, 1997
Recurrence risk figures for isolated tetralogy of Fallot after screening for 22q11 microdeletionM C Digilio, B Marino, A Giannotti, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|April 29, 2006
22q11 deletion syndrome: a review of some developmental biology aspects of the cardiovascular systemAngelo Restivo, Anna Sarkozy, Maria Cristina Digilio, et al.
Clinical Dysmorphology|September 8, 2006
Concordant familial segregation of atrial septal defect and Axenfeld-Rieger anomaly in father and sonGiulio Calcagni, Maria Cristina Digilio, Rossella Capolino, et al.
European Journal of Pediatrics|November 9, 2006
Familial recurrence of congenital heart disease: an overview and review of the literatureGiulio Calcagni, M Cristina Digilio, Anna Sarkozy, et al.
American Journal of Medical Genetics. Part A|September 11, 2010
Shells and heart: are human laterality and chirality of snails controlled by the same maternal genes?Marco Oliverio, Maria Cristina Digilio, Paolo Versacci, 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.
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