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Autore Titolo Tipo [ Anno] Filtri: First Letter Of Title è C and Autore is Fabretto, Antonella [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.
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