Authors:
BARANZINI SE
GILIBERTO F
HERRERA M
BERNATH V
BARREIRO C
ERRO MG
GRIPPO J
SZIJAN I
Citation: Se. Baranzini et al., DELETION PATTERNS IN ARGENTINE PATIENTS WITH DUCHENNE AND BECKER MUSCULAR-DYSTROPHY, Neurological research, 20(5), 1998, pp. 409-414
Authors:
DIFULVIO M
CHIESA AE
BARANZINI SE
GRUNIEROPAPENDIECK L
MASINIREPISO AM
TARGOVNIK HM
Citation: M. Difulvio et al., A NEW POINT MUTATION (M313T) IN THE THYROID-HORMONE RECEPTOR-BETA GENE IN A PATIENT WITH RESISTANCE TO THYROID-HORMONE, Thyroid, 7(1), 1997, pp. 43-44
Authors:
BARANZINI SE
DELREY G
NIGRO N
SZIJAN I
CHAMOLES N
CRESTO JC
Citation: Se. Baranzini et al., PATIENT WITH AN XP21 CONTIGUOUS GENE DELETION SYNDROME IN ASSOCIATIONWITH AGENESIS OF THE CORPUS-CALLOSUM, American journal of medical genetics, 70(3), 1997, pp. 216-221
Citation: Se. Baranzini et al., 4 NEW POLYMORPHISMS IN THE HUMAN DYSTROPHIN GENE FROM AN ARGENTINEAN POPULATION, Muscle & nerve, 20(11), 1997, pp. 1451-1453