Showing results (121-130 of 527) with videos related to

Sort By:
Pageof 53
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology|April 3, 2002
[Transposition of great arteries. Understanding its pathogenesis]Bruno Marino, M Cristina Digilio, Paolo Versacci, et al.
International Journal of Pediatric Otorhinolaryngology|December 2, 2019
Genetic identification and molecular modeling characterization of a novel POU3F4 variant in two Italian deaf brothersSara Giannantonio, Emanuele Agolini, Alessandro Scorpecci, et al.
Frontiers in Plant Science|January 25, 2021
Zucchini Plants Alter Gene Expression and Emission of (E)-β-Caryophyllene Following Aphis gossypii InfestationAlessia Vitiello, Donata Molisso, Maria Cristina Digilio, et al.
The Journal of Thoracic and Cardiovascular Surgery|August 25, 2009
Impact of DEL22q11, trisomy 21, and other genetic syndromes on surgical outcome of conotruncal heart defectsGuido Michielon, Bruno Marino, Gianluca Oricchio, et al.
European Journal of Cardio-Thoracic Surgery : Official Journal of the European Association for Cardio-Thoracic Surgery|December 19, 2008
Genetic syndromes and congenital heart defects: how is surgical management affected?Roberto Formigari, Guido Michielon, Maria Cristina Digilio, et al.
American Journal of Medical Genetics. Part A|March 26, 2014
Holt-Oram syndrome with intermediate atrioventricular canal defect, and aortic coarctation: functional characterization of a de novo TBX5 mutationAnwar Baban, Letizia Pitto, Silvia Pulignani, et al.
Human Molecular Genetics|April 25, 2015
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the ciliumJosé A Caparrós-Martín, Alessandro De Luca, François Cartault, et al.
Human Mutation|February 20, 2004
A homozygous GJA1 gene mutation causes a Hallermann-Streiff/ODDD spectrum phenotypeAntonio Pizzuti, Elisabetta Flex, Rita Mingarelli, et al.
BMC Health Services Research|March 19, 2016
Survey of medical genetic services in Italy: year 2011Daniela Giardino, Rita Mingarelli, Tiziana Lauretti, et al.
Haematologica|January 19, 2007
Sequence-specific modification of a beta-thalassemia locus by small DNA fragments in human erythroid progenitor cellsAlessia Colosimo, Valentina Guida, Ivana Antonucci, et al.
Pageof 53