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

American journal of medical genetics

Baranzini SE, del Rey G, Nigro N, Szijan I, Chamoles N, Cresto JC. Patient with an Xp21 contiguous gene deletion syndrome in association with agenesis of the corpus callosum. Am J Med Genet. 1997 Jun 13; 70(3):216-21.

1997
https://researcherprofiles.org/profile/1404351
9188656

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