The facial dysmorphology analysis technology in intellectual disability syndromes related to defects in the histones modifiersGiulia Pascolini, Paola Grammatico, Nicole Fleischer et al.|Journal of Human Genetics|2019Cited by 11
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletionGiulia Pascolini, Paola Grammatico, Michele Valiante et al.|European Journal of Medical Genetics|2019Cited by 9
Koolen‐de Vries syndrome in the first adulthood patient of Southern India ancestryGiulia Pascolini, Paola Grammatico, Federica Gaudioso et al.|American Journal of Medical Genetics Part A|2020Cited by 3