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المؤلفون: Grugni, G, Crinò, A, Bosio, L, Corrias, A, Cuttini, M, DE TONI, T, DI BATTISTA, E, Franzese, A, Gargantini, L, Greggio, N, Iughetti, Lorenzo, Livieri, C, Naselli, A, Pagano, C, Pozzan, G, Ragusa, L, Salvatoni, A, Trifirò, G, Beccaria, L, Bellizzi, M, Bellone, J, Brunani, A, Cappa, M, Caselli, G, Cerioni, V, Delvecchio, M, Giardino, D, Iannì, F, Memo, L, Pilotta, A, Pomara, C, Radetti, G, Sacco, M, Sanzari, A, Sartorio, A, Tonini, G, Vettor, R, Zaglia, F, Chiumello, G, GENETIC OBESITY STUDY GROUP OF ITALIAN SOCIETY OF PEDIATRIC ENDOCRINOLOGY AND DIABETOLOGY ISPED
مصطلحات موضوعية: Adult, Male, obesity, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Pediatrics, Epidemiologic study, Adolescent, Body Mass Index, Chromosome 15, death, Internal medicine, Epidemiology, Genetics, medicine, Humans, Obesity, Child, Genetics (clinical), In Situ Hybridization, Fluorescence, Cause of death, Chromosomes, Human, Pair 15, business.industry, Mortality rate, Prader-Willi syndrome, GH therapy, nutritional and metabolic diseases, Respiratory infection, Infant, Middle Aged, medicine.disease, Death, Endocrinology, Italy, Child, Preschool, Growth Hormone, Female, Risk of death, business, Prader-Willi Syndrome, Prader-Willi syndrome, obesity, GH therapy, death
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df3c0c2468dddea8d51d82c16f4b976a
http://hdl.handle.net/11577/2430423