Copy number variation (CNV) identification, interpretation, and database from Brazilian patients-Reference-Cited by-同舟云学术

Copy number variation (CNV) identification, interpretation, and database from Brazilian patients

Published:2020 Issue:4 Volume:43 Page:
ISSN:1678-4685
Container-title:Genetics and Molecular Biology
language:
Short-container-title:Genet. Mol. Biol.

Author:

Godoy Victória Cabral Silveira Monteiro de¹,Bellucco Fernanda Teixeira¹,Colovati Mileny¹,Oliveira-Junior Hélio Rodrigues de¹,Moysés-Oliveira Mariana¹,Melaragno Maria Isabel¹^ORCID

Affiliation:

1. Universidade Federal de São Paulo, Brazil

Publisher

FapUNIFESP (SciELO)

Subject

Genetics,Molecular Biology

Link

http://www.scielo.br/pdf/gmb/v43n4/1678-4685-GMB-43-4-e20190218.pdf

Reference42 articles.

1. Genome structural variation discovery and genotyping;Alkan C;Nat Rev Genet,2011

2. Estimating Asian contribution to the Brazilian population: A new application of a validated set of 61 ancestry informative markers;Andrade RB;G3 Genes/Genomes/Genetics,2018

3. Refining analyses of copy number variation identifies specific genes associated with developmental delay;Coe BP;Nat Genet,2014

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