Marίa Eugenia Foncuberta

3PUBLICATIONS
25CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsNeurology and neuromuscular diseasesNanomedicine
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Publications (3)

|Sep 14, 2026
Molecular diagnosis of spinal muscular atrophy: Experience in a pediatric hospital in Argentina.

|Aug 18, 2026
Clinical, Histological, and Genetic Characterization of a Large Cohort of 49 Patients With Nebulin-Related Congenital Myopathy.

|Jun 11, 2022
Challenges in genetic diagnosis, co-occurrence of 22q11.2 deletion syndrome and Noonan syndrome.

Josefina Chinton, Victoria Huckstadt, Maria Eugenia Foncuberta

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Frequent Collaborators

2 joint publications

Josefina Chinton

2 joint publications

Victoria Huckstadt

2 joint publications

María Gabriela Obregon

2 joint publications

Soledad Monges