Export 3 results: 
 Autore  Titolo  Tipo  [ Anno
] Filtri: Autore è Faletra, Flavio and First Letter Of Title is C  [Clear All Filters]
. A Case of Prenatal Neurocytoma Associated With ATR-16 Syndrome. J Ultrasound Med 2016;35(6):1359-61.
. Contribution of SNP arrays in diagnosis of deletion 2p11.2-p12. Gene 2012;492(1):315-8.
. A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation. Ophthalmic Genet 2010;31(2):98-100.