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:
ORLOW I
LACOMBE L
PELLICER I
RABBANI F
DELGADO R
ZHANG ZF
SZIJAN I
CORDONCARDO C
Citation: I. Orlow et al., GENOTYPIC AND PHENOTYPIC CHARACTERIZATION OF THE HISTOBLOOD GROUP ABO(H) IN PRIMARY BLADDER-TUMORS, International journal of cancer, 75(6), 1998, pp. 819-824
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
Authors:
SZIJAN I
LOHMANN DR
PARMA DL
BRANDT B
HORSTHEMKE B
Citation: I. Szijan et al., IDENTIFICATION OF RB1 GERMLINE MUTATIONS IN ARGENTINEAN FAMILIES WITHSPORADIC BILATERAL RETINOBLASTOMA, Journal of Medical Genetics, 32(6), 1995, pp. 475-479