Juliana Alves Josahkian

3PUBLICATIONS
28CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Epidemiological methodsDevelopmental genetics (incl. sex determination)
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Publications (3)

|May 07, 2021
Genotype-phenotype studies in a large cohort of Brazilian patients with Hunter syndrome.

Juliana Alves Josahkian, Ana Carolina Brusius-Facchin, Alice Brinckmann Oliveira Netto

|Jan 27, 2021
Updated birth prevalence and relative frequency of mucopolysaccharidoses across Brazilian regions.

Juliana Alves Josahkian, Franciele Barbosa Trapp, Maira Graeff Burin

|Aug 01, 2020
Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.

Bruna Lixinski Diniz, Andressa Schneiders Santos, Andressa Barreto Glaeser

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Frequent Collaborators

2 joint publications

Sandra Leistner-Segal

2 joint publications

Roberto Giugliani

1 joint publications

Bruna Lixinski Diniz

1 joint publications

Andressa Schneiders Santos