Helena Fabbri-Scallet
6PUBLICATIONS
24CO-AUTHORS
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Publications (6)
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|May 27, 2023
DHX37 and NR5A1 Variants Identified in Patients with 46,XY Partial Gonadal Dysgenesis.Felipe Rodrigues de Oliveira, Taís Nitsch Mazzola, Maricilda Palandi de Mello
|Nov 30, 2022
Clinical and laboratory differences between chromosomal and undefined causes of non-obstructive azoospermia: A retrospective study.Luísa Riccetto, Tarsis Paiva Vieira, Nilma Lucia Viguetti-Campos
|Oct 11, 2022
Sex dimorphism of weight and length at birth: evidence based on disorders of sex development.D S R Amais, T E R da Silva, B A Barros
|Aug 26, 2022
MYRF: A New Regulator of Cardiac and Early Gonadal Development-Insights from Single Cell RNA Sequencing Analysis.Verónica Calonga-Solís, Helena Fabbri-Scallet, Fabian Ott
|Sep 13, 2019
Mutation update for the NR5A1 gene involved in DSD and infertility.Helena Fabbri-Scallet, Lizandra Maia de Sousa, Andréa Trevas Maciel-Guerra
|Oct 14, 2017
Functional characterization of five NR5A1 gene mutations found in patients with 46,XY disorders of sex development.Helena Fabbri-Scallet, Maricilda Palandi de Mello, Gil Guerra-Júnior
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Frequent Collaborators
4 joint publications
Andréa Trevas Maciel-Guerra
4 joint publications
Maricilda Palandi de Mello
3 joint publications
Gil Guerra-Júnior
2 joint publications
Ralf Werner
2 joint publications
Olaf Hiort
2 joint publications
Antonia Paula Marques-de-Faria
2 joint publications
Tais Nitsch Mazzola
2 joint publications
Mara Sanches Guaragna
2 joint publications
Tarsis Paiva Vieira
2 joint publications
Nilma Lucia Viguetti-Campos
