Publications

Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.

Baranzini SE, Giliberto F, Dalamon V, Barreiro C, García-Erro M, Grippo J, Szijan I

Clinical genetics, 1998

Deletion patterns in Argentine patients with Duchenne and Becker muscular dystrophy.

Baranzini SE, Giliberto F, Herrera M, Bernath V, Barreiro C, Garcia Erro M, Grippo J, Szijan I

Neurological research, 1998

Clinical, cytogenetic, and molecular testing of Argentine patients with retinoblastoma.

Arbetman A, Abdala M, Fandiño A, Herrera J, Baranzini S, Borelina D, Parma D, Manzitti J, Barreiro C, Giliberto F, Szijan I

Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus, 1998

Four new polymorphisms in the human dystrophin gene from an Argentinian population.

Baranzini SE, Lenk U, Szijan I, Speer A

Muscle & nerve, 1997

Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum.

Baranzini SE, del Rey G, Nigro N, Szijan I, Chamoles N, Cresto JC

American journal of medical genetics, 1997

A new point mutation (M313T) in the thyroid hormone receptor beta gene in a patient with resistance to thyroid hormone.

di Fulvio M, Chiesa AE, Baranzini SE, Gruñiero-Papendieck L, Masini-Repiso AM, Targovnik HM

Thyroid : official journal of the American Thyroid Association, 1997

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