Publications by authors named "Janaina Huber"

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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, Bruna Baierle Guaraná, Cláudia Fernandes Lorea, Janaína Huber

J Pediatr Genet· December 2020

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Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects.
Karen Regina de Souza, Rafaella Mergener, Janaina Huber, Lucia Campos Pellanda, Mariluce Riegel

Biomed Res Int· March 2016

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Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Janaína Huber, Vivian Catarino Peres, Alexandre Luz de Castro, Tiago Jeronimo dos Santos, Lauro da Fontoura Beltrão

Pediatr Cardiol· December 2014

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Congenital heart diseases in a reference service: clinical evolution and associated illnesses.
Janaína Huber, Vivian Catarino Peres, Tiago Jeronimo dos Santos, Lauro da Fontoura Beltrão, Angélica Cerveira de Baumont

Arq Bras Cardiol· March 2010

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Cardiac surgery unmasks latent hypoparathyroidism in a child with the 22q11.2 deletion syndrome.
Beatriz D'Agord Schaan, Janaina Huber, Julio Cesar L Leite, Andrea Kiss

J Pediatr Endocrinol Metab· July 2006

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