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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Dettagli Bibliografici
Pubblicato in:J Mol Diagn
Autori principali: Jobanputra, Vaidehi, Andrews, Peter, Felice, Vanessa, Abhyankar, Avinash, Kozon, Lukasz, Robinson, Dino, London, Ferrah, Hakker, Inessa, Wrzeszczynski, Kazimierz, Ronemus, Michael
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Society for Investigative Pathology 2020
Soggetti:
Regular Article
Accesso online: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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