L. Flagiello

A synaptobrevin–like gene in the Xq28 pseudoautosomal region undergoes X inactivation

M. D'Esposito, A. Ciccodicola, F. Gianfrancesco, 1996, Nature Genetics.

Autosomal-dominant retinitis pigmentosa associated with an Arg-135-Trp point mutation of the rhodopsin gene. Clinical features and longitudinal observations.

L. Flagiello, E. Vingolo, M. Pannarale, 1996, Ophthalmology.

Mutation in the nerve-specific 5'non-coding region of Cx32 gene and absence of specific mRNA in a CMTX1 Italian family. Mutations in brief no. 195. Online.

M. D'Esposito, A. Ciccodicola, L. Flagiello, 1998, Human mutation.

Ocular signs associated with a rhodopsin mutation (Cys-167→Arg) in a family with autosomal dominant retinitis pigmentosa

A. Ciccodicola, L. Flagiello, M. D'urso, 1998, The British journal of ophthalmology.

Expressed STSs and transcription of human Xq28.

M. D'Esposito, A. Ciccodicola, T. Esposito, 1997, Gene.

Autosomal-dominant Retinitis Pigrnentosa Associated with an Arg-135-Trp Point Mutation of the Rhodopsin Gene

L. Flagiello, E. Vingolo, M. Pannarale, 1996 .

Autosomal ... dominant Retinitis Pigmentosa Associated with an

L. Flagiello, E. Vingolo, B. Grammatico, 1996 .