Maricilda Palandi de Mello

13PUBLICATIONS
55CO-AUTHORS
Medical genetics (excl. cancer genetics)Developmental genetics (incl. sex determination)Medical biochemistry - nucleic acidsAdolescent healthNeonatology
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Publications (13)

|Oct 18, 2024
Insights from a Wolfram syndrome cohort: clinical and molecular findings from a specialized diabetes reference center.

Carolina Paniago Lopes, Gentil Ferreira Gonçalves, Maria Fernanda Vanti Macedo Paulino

|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

|Jan 08, 2023
A Novel Look at Dosage-Sensitive Sex Locus Xp21.2 in a Case of 46,XY Partial Gonadal Dysgenesis without NR0B1 Duplication.

Ana Paula Francese-Santos, Jakob A Meinel, Cristiane S C Piveta

|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

|Feb 09, 2022
Leydig and Sertoli cell function in individuals with genital ambiguity, 46,XY karyotype, palpable gonads and normal testosterone secretion: a case-control study.

Guilherme Guaragna-Filho, Antônio Ramos Calixto, Anna Beatriz Lima do Valle Astur

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