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Paola Cerruti Mainardi

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Orphanet Journal of Rare Diseases|September 7, 2006
Cri du Chat syndromePaola Cerruti Mainardi
Orphanet Journal of Rare Diseases|October 26, 2007
Mowat-Wilson syndromeLivia Garavelli, Paola Cerruti Mainardi
European Journal of Pediatrics|May 14, 2011
Infantile cortical hyperostosis and COL1A1 mutation in four generationsPaola Cerruti-Mainardi, Giacomo Venturi, Marianna Spunton, et al.
European Journal of Medical Genetics|February 14, 2006
The natural history of Cri du Chat Syndrome. A report from the Italian RegisterPaola Cerruti Mainardi, Guido Pastore, Chiara Castronovo, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotypeDuccio Maria Cordelli, Livia Garavelli, Salvatore Savasta, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Orphanet Journal of Rare Diseases|September 7, 2006
Cri du Chat syndromePaola Cerruti Mainardi
Orphanet Journal of Rare Diseases|October 26, 2007
Mowat-Wilson syndromeLivia Garavelli, Paola Cerruti Mainardi
European Journal of Pediatrics|May 14, 2011
Infantile cortical hyperostosis and COL1A1 mutation in four generationsPaola Cerruti-Mainardi, Giacomo Venturi, Marianna Spunton, et al.
European Journal of Medical Genetics|February 14, 2006
The natural history of Cri du Chat Syndrome. A report from the Italian RegisterPaola Cerruti Mainardi, Guido Pastore, Chiara Castronovo, et al.
American Journal of Medical Genetics. Part A|January 17, 2013
Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotypeDuccio Maria Cordelli, Livia Garavelli, Salvatore Savasta, et al.
Pageof 1