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Results: 4

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

Authors: BARANZINI SE LENK U SZIJAN I SPEER A
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
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