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Page 1
Oncologic causes of precocious puberty.
Perilongo G, Rigon F, Murgia A. Perilongo G, et al. Among authors: murgia a. Pediatr Hematol Oncol. 1989;6(4):331-40. doi: 10.3109/08880018909034304. Pediatr Hematol Oncol. 1989. PMID: 2701702 Review.
Characterization of intellectual disability and autism comorbidity through gene panel sequencing.
Aspromonte MC, Bellini M, Gasparini A, Carraro M, Bettella E, Polli R, Cesca F, Bigoni S, Boni S, Carlet O, Negrin S, Mammi I, Milani D, Peron A, Sartori S, Toldo I, Soli F, Turolla L, Stanzial F, Benedicenti F, Marino-Buslje C, Tosatto SCE, Murgia A, Leonardi E. Aspromonte MC, et al. Among authors: murgia a. Hum Mutat. 2019 Sep;40(9):1346-1363. doi: 10.1002/humu.23822. Epub 2019 Aug 2. Hum Mutat. 2019. PMID: 31209962 Free PMC article.
Connexin 26 deafness is not always congenital.
Orzan E, Murgia A. Orzan E, et al. Among authors: murgia a. Int J Pediatr Otorhinolaryngol. 2007 Mar;71(3):501-7. doi: 10.1016/j.ijporl.2006.12.002. Epub 2007 Jan 11. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17222463
Molecular diagnosis of inherited diseases.
Murgia A, Polli R, Martella M, Vinanzi C, Opocher G. Murgia A, et al. Clin Chim Acta. 1999 Feb;280(1-2):73-80. doi: 10.1016/s0009-8981(98)00199-5. Clin Chim Acta. 1999. PMID: 10090525 Review.
Somatic mosaicism in von Hippel-Lindau Disease.
Murgia A, Martella M, Vinanzi C, Polli R, Perilongo G, Opocher G. Murgia A, et al. Hum Mutat. 2000 Jan;15(1):114. doi: 10.1002/(SICI)1098-1004(200001)15:1<114::AID-HUMU20>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10612832
239 results