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American Journal of Medical Genetics. Part A|September 12, 2006
Familial occurrence of multiple pterygium syndrome: expression in a heterozygote of the recessive form or variability of the dominant form?Paolo Prontera, Alberto Sensi, Luciano Merlo, et al.
Acta Paediatrica (Oslo, Norway : 1992)|August 31, 2007
Immunological patterns in young children with Down syndrome: is there a temporal trend?Guido Cocchi, Maura Mastrocola, Marilu' Capelli, et al.
The Journal of Pediatrics|February 24, 2006
Starch thickening of human milk is ineffective in reducing the gastroesophageal reflux in preterm infants: a crossover study using intraluminal impedanceLuigi Corvaglia, Marianna Ferlini, Raffaella Rotatori, et al.
Fetal Diagnosis and Therapy|January 24, 2015
Prenatal diagnosis of open spina bifida in Emilia-RomagnaTullio Ghi, Guido Cocchi, Letizia Conti, et al.
American Journal of Medical Genetics. Part A|September 17, 2013
Silver-Russell syndrome due to paternal H19/IGF2 hypomethylation in a twin girl born after in vitro fertilizationGuido Cocchi, Concetta Marsico, Anita Cosentino, et al.
Dermatology Practical & Conceptual|August 7, 2019
Disseminate Recurrent Folliculitis and Hidradenitis Suppurativa Are Associated Conditions: Results From a Retrospective Study of 131 Patients With Down Syndrome and a Cohort of 12,351 Pediatric ControlsAndrea Sechi, Alba Guglielmo, Annalisa Patrizi, et al.
American Journal of Medical Genetics. Part A|June 30, 2016
Oro-dental features of Pallister-Killian syndrome: Evaluation of 21 European probandsSimone Bagattoni, Giovanni D'Alessandro, Agnese Sadotti, et al.
Frontiers in Nutrition|September 27, 2021
Eating and Lifestyle Habits in Youth With Down Syndrome Attending a Care Program: An Exploratory Lesson for Future ImprovementsGiulia Roccatello, Guido Cocchi, Rosa Tullia Dimastromatteo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 11, 2019
Myoclonic epilepsy with photosensitivity in infants with Pallister-Killian SyndromeEmilia Ricci, Rocco Bonfatti, Alessandro Rocca, et al.
Frontiers in Genetics|May 10, 2018
Integrated Quantitative Transcriptome Maps of Human Trisomy 21 Tissues and CellsMaria Chiara Pelleri, Chiara Cattani, Lorenza Vitale, et al.
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