Detailed phenotype–genotype study in five patients with chromosome 6q16 deletion: narrowing the critical region for Prader–Willi-like phenotype
María Clara Bonaglia(IRCCS Eugenio Medea), Roberto Ciccone(University of Pavia), Giorgio Gimelli(Istituto Giannina Gaslini), Stefania Gimelli(University of Pavia), Susan Marelli(IRCCS Eugenio Medea), Joke Verheij(University Medical Center Groningen), Roberto Giorda(IRCCS Eugenio Medea), Rita Grasso(IRCCS Eugenio Medea), Renato Borgatti(IRCCS Eugenio Medea), Filomena Pagone(Hospital Universitari Sant Joan de Reus), Laura Rodríguez(Instituto de Salud Carlos III), Maria-Luisa Martinez-Frias(Universidad San Pablo CEU), Conny van Ravenswaaij(University Medical Center Groningen), Orsetta Zuffardi(University of Pavia)
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