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Epigenetics|April 24, 2014
Overall and allele-specific expression of the SMC1A gene in female Cornelia de Lange syndrome patients and healthy controlsIlaria Parenti, Davide Rovina, Maura Masciadri, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 5, 2016
Sedation and general anesthesia for patients with Cornelia De Lange syndrome: A case seriesAlessandra Moretto, Vittorio Scaravilli, Valentina Ciceri, et al.
American Journal of Medical Genetics. Part A|April 5, 2025
Cohesins: Crossroad Between Cornelia de Lange Spectrum and Cancer PredispositionLaura Rigotti, Stefano Rebellato, Antonella Lettieri, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Otitis media with effusion and hearing loss in children with Cornelia de Lange syndromePaola Marchisio, Angelo Selicorni, Lorenzo Pignataro, et al.
American Journal of Medical Genetics. Part A|December 22, 2023
Double somatic mosaicism in Cornelia de Lange syndromeLidia Pezzani, Laura Pezzoli, Erica Rosina, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Prevalence of Beckwith-Wiedemann syndrome in North West of ItalyAlessandro Mussa, Silvia Russo, Agostina De Crescenzo, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 24, 2009
Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single familyLaura Cardarelli, Angela Sparago, Agostina De Crescenzo, et al.
European Journal of Human Genetics : EJHG|February 4, 2010
High frequency of copy number imbalances in Rubinstein-Taybi patients negative to CREBBP mutational analysisCristina Gervasini, Federica Mottadelli, Roberto Ciccone, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 11, 2016
Adolescents and adults affected by Cornelia de Lange syndrome: A report of 73 Italian patientsMilena Mariani, Valentina Decimi, Laura Rachele Bettini, et al.
European Journal of Human Genetics : EJHG|July 9, 2004
A double cryptic chromosome imbalance is an important factor to explain phenotypic variability in Wolf-Hirschhorn syndromeMarcella Zollino, Rosetta Lecce, Angelo Selicorni, et al.
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