Pelizzo, G.; Chiricosta, L.; Mazzon, E.; Zuccotti, G.V.; Avanzini, M.A.; Croce, S.; Lima, M.; Bramanti, P.; Calcaterra, V.
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatr. Rep. 2021, 13, 45-56.
https://doi.org/10.3390/pediatric13010006
AMA Style
Pelizzo G, Chiricosta L, Mazzon E, Zuccotti GV, Avanzini MA, Croce S, Lima M, Bramanti P, Calcaterra V.
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric Reports. 2021; 13(1):45-56.
https://doi.org/10.3390/pediatric13010006
Chicago/Turabian Style
Pelizzo, Gloria, Luigi Chiricosta, Emanuela Mazzon, Gian Vincenzo Zuccotti, Maria Antonietta Avanzini, Stefania Croce, Mario Lima, Placido Bramanti, and Valeria Calcaterra.
2021. "Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention" Pediatric Reports 13, no. 1: 45-56.
https://doi.org/10.3390/pediatric13010006
APA Style
Pelizzo, G., Chiricosta, L., Mazzon, E., Zuccotti, G. V., Avanzini, M. A., Croce, S., Lima, M., Bramanti, P., & Calcaterra, V.
(2021). Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric Reports, 13(1), 45-56.
https://doi.org/10.3390/pediatric13010006
