A citation-based method for searching scientific literature

Robert J Shprintzen. Dev Disabil Res Rev 2008
Times Cited: 271



Caterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, Annarosa Soresina, Silvana Martino, Roberto Rondelli, Rita Consolini, Ezia Maria Ruga, Fabio Cardinale, Andrea Finocchi, Maria Luisa Romiti, Baldassarre Martire, Rosa Bacchetta, Veronica Albano, Adriano Carotti, Fernando Specchia, Davide Montin, Emilia Cirillo, Guido Cocchi, Antonino Trizzino, Grazia Bossi, Ornella Milanesi, Chiara Azzari, Giovanni Corsello, Claudio Pignata, Alessandro Aiuti, Maria Cristina Pietrogrande, Bruno Marino, Alberto Giovanni Ugazio, Alessandro Plebani, Paolo Rossi. J Pediatr 2014
Times Cited: 78




List of shared articles



Times cited

The Oral Health of Patients with DiGeorge Syndrome (22q11) Microdeletion: A Case Report.
Estephania Candelo, Maria Alejandra Estrada-Mesa, Adriana Jaramillo, Carlos Humberto Martinez-Cajas, Julio Cesar Osorio, Harry Pachajoa. Appl Clin Genet 2021
0

CNVs in the 22q11.2 Chromosomal Region Should Be an Early Suspect in Infants with Congenital Cardiac Disease.
Tatiana Pineda, Ignacio Zarante, Angela Camila Paredes, Juan Pablo Rozo, Martha C Reyes, Olga María Moreno-Niño. Clin Med Insights Cardiol 2021
0

Age-dependent expression pattern in the mammalian brain of a novel, small peptide encoded in the 22q11.2 deletion syndrome region.
Sabrina Kragness, Mark A A Harrison, Joby J Westmoreland, Adam Burstain, Laurie R Earls. Gene Expr Patterns 2018
0

Modeling age-specific facial development in Williams-Beuren-, Noonan-, and 22q11.2 deletion syndromes in cohorts of Czech patients aged 3-18 years: A cross-sectional three-dimensional geometric morphometry analysis of their facial gestalt.
Martina Čaplovičová, Veronika Moslerová, Ján Dupej, Milan Macek, Dana Zemková, Eva Hoffmannová, Markéta Havlovicová, Jana Velemínská. Am J Med Genet A 2018
0

A Comprehensive Craniofacial Study of 22q11.2 Deletion Syndrome.
A Lewyllie, J Roosenboom, K Indencleef, P Claes, A Swillen, K Devriendt, C Carels, M Cadenas De Llano-Pérula, G Willems, G Hens,[...]. J Dent Res 2017
10

"FISHed" out the diagnosis: A case of DiGeorge syndrome.
S Bajaj, T S Thombare, M S Tullu, M Agrawal. J Postgrad Med 2016
0

Fluency aspects of oral narrative task in del22q11.2 syndrome.
Amanda Oliveira Santos, Natalia Freitas Rossi, Maria da Conceição Faria Freitas Tandel, Antonio Richieri-Costa, Célia Maria Giacheti. Codas 2016
1