Paula Scaglia
3PUBLICATIONS
13CO-AUTHORS
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Publications (3)
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|Jan 28, 2026
46,XY DSD with Partial Gonadal Dysgenesis and Growth Failure in a Patient with 3q27.1 Microdeletion: Candidate Gene Curation After Exhaustive Literature Review.Lourdes Correa Brito, Sofía Suco, Bárbara Casali
|Jul 29, 2023
Identification of a Novel Variant in Myelin Regulatory Growth Factor by Next-Generation Sequencing Led to the Detection of a Clinically Inapparent Congenital Heart Defect in a Patient with a 46,XY Disorder of Sex Development.Lourdes Correa Brito, Romina P Grinspon, Jimena Lopez Dacal
|Jun 06, 2019
A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING.Maria de Fátima Borges, Horacio Mario Domené, Paula Alejandra Scaglia
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Frequent Collaborators
2 joint publications
Lourdes Correa Brito
2 joint publications
Rodolfo A Rey
1 joint publications
Maria de Fátima Borges
1 joint publications
Horacio Mario Domené
1 joint publications
Beatriz Hallal Jorge Lara
1 joint publications
Heloísa Marcelina da Cunha Palhares
1 joint publications
Andréia Vasconcelos Aguiar Santos
1 joint publications
Amanda Lacerda Ferreira Gonçalves
1 joint publications
Marília Matos Oliveira
1 joint publications
Alessandra Bernadete Trovó de Marqui
