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Journal of Andrology|April 21, 2012
A unique patient presenting with concomitant Klinefelter syndrome, Alport syndrome, and craniopharyngiomaMario Rotondi, Chiara Fallerini, Barbara Pirali, et al.
Genes|October 23, 2021
Autism Spectrum Disorders: Analysis of Mobile Elements at 7q11.23 Williams-Beuren Region by Comparative GenomicsFrancesca Anna Cupaioli, Chiara Fallerini, Maria Antonietta Mencarelli, et al.
Animal : an International Journal of Animal Bioscience|March 27, 2012
Genetics of fibre production and fleece characteristics in small ruminants, Angora rabbit and South American camelidsD Allain, C Renieri
Clinical Dysmorphology|October 18, 2016
Combined ultrasound and exome sequencing approach recognizes Opitz G/BBB syndrome in two malformed fetusesAnna Maria Pinto, Valentina Imperatore, Laura Bianciardi, et al.
European Journal of Medical Genetics|February 9, 2019
MEIS2 gene is responsible for intellectual disability, cardiac defects and a distinct facial phenotypeAnnarita Giliberti, Aurora Currò, Filomena Tiziana Papa, et al.
Optics Letters|September 15, 2009
Evidence for multistability of light solitons in SF(6) absorption measurementsG Dattoli, F P Orsitto, A Torre
Cellular Reprogramming|June 9, 2025
Reprogramming of Different Cell Lineages into Functional β-Cell SubstitutesAnna A Dattoli, Yosip Kelemen, Xiaofeng Huang
International Journal of Molecular Sciences|March 2, 2016
Potentially Treatable Disorder Diagnosed Post Mortem by Exome Analysis in a Boy with Respiratory DistressValentina Imperatore, Maria Antonietta Mencarelli, Chiara Fallerini, et al.
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