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Anna Cereda

Showing results (11-20 of 55) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 8, 2014
Communication, cognitive development and behavior in children with Cornelia de Lange Syndrome (CdLS): preliminary resultsPaola Francesca Ajmone, Claudia Rigamonti, Francesca Dall'Ara, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patientsMaria Francesca Bedeschi, Vera Bianchi, Anna Maria Colli, et al.
American Journal of Medical Genetics. Part A|January 24, 2013
A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotypeChiara Castronovo, Daniela Rusconi, Milena Crippa, et al.
European Journal of Medical Genetics|January 15, 2013
Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotypeCristina Gervasini, Ilaria Parenti, Chiara Picinelli, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 6, 2016
A new prognostic index of severity of intellectual disabilities in Cornelia de Lange syndromeAnna Cereda, Milena Mariani, Paola Rebora, et al.
American Journal of Medical Genetics. Part A|September 22, 2018
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohortValentina Decimi, Barbara Parma, Roberto Panceri, et al.
Journal of Autism and Developmental Disorders|November 9, 2021
Neuropsychiatric Functioning in CDLS: A Detailed Phenotype and Genotype CorrelationPaola Francesca Ajmone, Beatrice Allegri, Anna Cereda, et al.
American Journal of Medical Genetics. Part A|October 7, 2015
Thrombocytopenia and Cornelia de Lange syndrome: Still an enigma?Valeria Cavalleri, Laura R Bettini, Chiara Barboni, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Cervical spine malformation in cornelia de lange syndrome: a report of three patientsLaura Rachele Bettini, Laura Locatelli, Milena Mariani, et al.
Epigenetics|June 11, 2015
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villiLeda Paganini, Nicole Carlessi, Laura Fontana, et al.
Pageof 6

Showing results (11-20 of 55) with videos related to

Sort By:
Pageof 6
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 8, 2014
Communication, cognitive development and behavior in children with Cornelia de Lange Syndrome (CdLS): preliminary resultsPaola Francesca Ajmone, Claudia Rigamonti, Francesca Dall'Ara, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patientsMaria Francesca Bedeschi, Vera Bianchi, Anna Maria Colli, et al.
American Journal of Medical Genetics. Part A|January 24, 2013
A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotypeChiara Castronovo, Daniela Rusconi, Milena Crippa, et al.
European Journal of Medical Genetics|January 15, 2013
Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotypeCristina Gervasini, Ilaria Parenti, Chiara Picinelli, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 6, 2016
A new prognostic index of severity of intellectual disabilities in Cornelia de Lange syndromeAnna Cereda, Milena Mariani, Paola Rebora, et al.
American Journal of Medical Genetics. Part A|September 22, 2018
Use of nutritional devices in Cornelia de Lange syndrome: Data from a large Italian cohortValentina Decimi, Barbara Parma, Roberto Panceri, et al.
Journal of Autism and Developmental Disorders|November 9, 2021
Neuropsychiatric Functioning in CDLS: A Detailed Phenotype and Genotype CorrelationPaola Francesca Ajmone, Beatrice Allegri, Anna Cereda, et al.
American Journal of Medical Genetics. Part A|October 7, 2015
Thrombocytopenia and Cornelia de Lange syndrome: Still an enigma?Valeria Cavalleri, Laura R Bettini, Chiara Barboni, et al.
American Journal of Medical Genetics. Part A|March 27, 2014
Cervical spine malformation in cornelia de lange syndrome: a report of three patientsLaura Rachele Bettini, Laura Locatelli, Milena Mariani, et al.
Epigenetics|June 11, 2015
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villiLeda Paganini, Nicole Carlessi, Laura Fontana, et al.
Pageof 6