Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies

Chromosomal microarray testing is indicated for patients with diagnoses including unexplained developmental delay or intellectual disability, autism spectrum disorders, and multiple congenital anomalies. The short multiply aggregated sequence homologies (SMASH) genomic assay is a novel next-generati...

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Bibliografische gegevens
Gepubliceerd in:J Mol Diagn
Hoofdauteurs: Jobanputra, Vaidehi, Andrews, Peter, Felice, Vanessa, Abhyankar, Avinash, Kozon, Lukasz, Robinson, Dino, London, Ferrah, Hakker, Inessa, Wrzeszczynski, Kazimierz, Ronemus, Michael
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Investigative Pathology 2020
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Regular Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7722526/
https://ncbi.nlm.nih.gov/pubmed/33132082
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jmoldx.2020.09.009
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