Bruna Lixinski Diniz

7PUBLICATIONS
21CO-AUTHORS
Neurology and neuromuscular diseasesDevelopmental genetics (incl. sex determination)Gene expression (incl. microarray and other genome-wide approaches)Fish pests and diseases
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Publications (7)

|Oct 22, 2025
Quality of life of adolescent, children and young adults with neurofibromatosis type 1: a scoping review.

Lucas Paulo de Souza, Bruna Lixinski Diniz, João Gabriel Toledo Medeiros

|Sep 11, 2024
Turner syndrome and neuropsychological abnormalities: a review and case series.

Bruna Baierle Guaraná, Marcela Rodrigues Nunes, Victória Feitosa Muniz

|Jul 27, 2024
Expanding the Phenotypic Spectrum of Pathogenic KIAA0586 Variants: From Joubert Syndrome to Hydrolethalus Syndrome.

Desirée Deconte, Bruna Lixinski Diniz, Jéssica K Hartmann

|Jul 12, 2023
Fluorescence in situ hybridization (FISH) as an irreplaceable diagnostic tool for Williams-Beuren syndrome in developing countries: a literature review.

Bianca Soares Carlotto, Desirée Deconte, Bruna Lixinski Diniz

|Apr 24, 2023
Congenital Heart Defects and 22q11.2 Deletion Syndrome: A 20-Year Update and New Insights to Aid Clinical Diagnosis.

Bruna Lixinski Diniz, Desirée Deconte, Kerolainy Alves Gadelha

|Sep 07, 2020
Candidate genes of oculo-auriculo-vertebral spectrum in 22q region: A systematic review.

Andressa Barreto Glaeser, Andressa Schneiders Santos, Bruna Lixinski Diniz

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