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pro vyhledávání: '"Katia Rocchetti"'
Autor:
Sau Wai Cheung, Katia Rocchetti, Chiara Pantaleoni, Pawel Stankiewicz, Maria Clara Bonaglia, Roberto Ciccone, Stefano D'Arrigo, Jeffrey R Hughes, Mary Bertrand, Thomy de Ravel, Nicola Brunetti-Pierri, Erika Della Mina, Christian P. Schaaf, Zhilian Xia, Naftha Jelluma, Orsetta Zuffardi, Renato Borgatti, Claudia A. L. Ruivenkamp, Parul Jayakar, Serena Belli, Alex R. Paciorkowski, V. Reid Sutton
Publikováno v:
European Journal of Human Genetics, 19(1), 102-107
Genome-wide high-resolution array analysis is rapidly becoming a reliable method of diagnostic investigation in individuals with mental retardation and congenital anomalies, leading to the identification of several novel microdeletion and microduplic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::200fbc29c64dcd4037a7753420903068
https://hdl.handle.net/1887/108675
https://hdl.handle.net/1887/108675
