Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls-Reference-Cited by-同舟云学术

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Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls

Published:2021-02 Issue:2 Volume:23 Page:280-288
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Bowling Kevin M.,Thompson Michelle L.,Gray David E.,Lawlor James M.J.,Williams Kelly,East Kelly M.,Kelley Whitley V.,Moss Irene P.,Absher Devin M.,Partridge E.Christopher,Hurst Anna C.E.,Edberg Jeffrey C.,Barsh Gregory S.,Korf Bruce R.,Cooper Gregory M.^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

https://www.nature.com/articles/s41436-020-00976-z.pdf

Reference30 articles.

1. Regalado A. More than 26 million people have taken an at-home ancestry test. 2019. https://www.technologyreview.com. Accessed 15 June 2020.

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