Andressa Barreto Glaeser

4PUBLICATIONS
92CO-AUTHORS
Developmental genetics (incl. sex determination)Respiratory diseases
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Publications (4)

|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 25, 2022
Hospital characteristics associated with COVID-19 mortality: data from the multicenter cohort Brazilian Registry.

Maira Viana Rego Souza-Silva, Patricia Klarmann Ziegelmann, Vandack Nobre

|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

|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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