Export 2 results:
Autore Titolo Tipo [ Anno
] Filtri: Autore è Fabretto, Antonella and First Letter Of Title is C [Clear All Filters]
. 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.