https://doi.org/10.7490/f1000research.1116018.1
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Chaves TF, Ocampos M, Barbato IT et al. Intragenic RBFOX1 deletions in patients with neurodevelopmental disorders: report of two cases [version 1; not peer reviewed]. F1000Research 2018, 7:1355 (poster) (https://doi.org/10.7490/f1000research.1116018.1)
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Intragenic RBFOX1 deletions in patients with neurodevelopmental disorders: report of two cases

Tiago Fernando Chaves1, Maristela Ocampos, Ingrid T. Barbato, Louise L. Pinto, Jorge H. Barbato Filho, Gisele R. de Luca, Angelica F. Maris
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Published 29 Aug 2018

Intragenic RBFOX1 deletions in patients with neurodevelopmental disorders: report of two cases

[version 1; not peer reviewed]

Tiago Fernando Chaves1, Maristela Ocampos, Ingrid T. Barbato, Louise L. Pinto, Jorge H. Barbato Filho, Gisele R. de Luca, Angelica F. Maris
Author Affiliations
1 UFSC, Brazil
Presented at
8th Cancer Genomics Consortium (CGC) Summer Meeting 2017
Abstract
Competing Interests

No competing interests were disclosed

Keywords
RBFOX1, aCGH, Microarray, neurodevelopmental, microdeletion
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