María Gabriela Obregon (María G Obregón, M G Obregon)

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 5

Top Topics

Clostridium Difficile

Top Venues

Archivos argentinos de pediatria

Journal of pediatric genetics

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Silvia Caino, Romina Alba, Silvina Bevilacqua, Mariana Roizen, María Gabriela Obregon, Virginia Fano
Osteochondromatosis: clinical variability and factors related to quality of life in children and adults. Archivos argentinos de pediatria 120 (3) (2022)
Rosario Ramos Mejía, Mariana Del Pino, M Aza-Carmona, Silvina Abbate, María Gabriela Obregon, Karen E Heath, Virginia Fano
Novel FLNB Variants in Seven Argentinian Cases with Spondylocarpotarsal Synostosis Syndrome. Journal of pediatric genetics 13 (3) (2022)
Josefina Chinton, Victoria Huckstadt, Maria Eugenia Foncuberta, Maria Mercedes Perez, Mara Cecilia Bonetto, Luis Pablo Gravina, María Gabriela Obregon
Challenges in genetic diagnosis, co-occurrence of 22q11.2 deletion syndrome and Noonan syndrome. American journal of medical genetics. Part A 188 (8) (2022)
M Agustina Valentini, Valeria A Fedrizzi, Gabriela Krochik, Silvina Abbate, Mariela Ferrari, Monica Beatriz Contreras, Soraya El Kik, M Beatriz Araujo, María Gabriela Obregon
DGAT1 mutation in two sisters with failure to thrive: a case report. Archivos argentinos de pediatria (2022)
Rosario Ramos Mejía, Mariana Del Pino, M Aza-Carmona, Silvina Abbate, María Gabriela Obregon, Karen E Heath, Virginia Fano
Novel FLNB Variants in Seven Argentinian Cases with Spondylocarpotarsal Synostosis Syndrome. Journal of pediatric genetics 13 (3) (2022)