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

Copy number variations (CNVs) constitute an important class of variation in the human genome and the interpretation of their pathogenicity considering different frequencies across populations is still a challenge for geneticists. Since the CNV databases are predominantly composed of European and non...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:Genet Mol Biol
Main Authors: de Godoy, Victória Cabral Silveira Monteiro, Bellucco, Fernanda Teixeira, Colovati, Mileny, de Oliveira-Junior, Hélio Rodrigues, Moysés-Oliveira, Mariana, Melaragno, Maria Isabel
Format: Artigo
Sprog:Inglês
Udgivet: Sociedade Brasileira de Genética 2020
Fag:
Human and Medical Genetics
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7783508/
https://ncbi.nlm.nih.gov/pubmed/33306777
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2019-0218
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker