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Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management

Crossref DOI link: https://doi.org/10.1038/s41436-019-0551-9

Published Print: 2019-11

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Sheppard, Sarah E.

Lalonde, Emilie

Adzick, N. Scott

Beck, Anita E.

Bhatti, Tricia

De Leon, Diva D.

Duffy, Kelly A.

Ganguly, Arupa

Hathaway, Evan

Ji, Jianling

Linn, Rebecca

Lord, Katherine

Randolph, Linda M.

Sajorda, Brian

States, Lisa

Conlin, Laura K.

Kalish, Jennifer M.
Funding

Funding for this research was provided by:

National Cancer Institute (CA193915)

Alex's Lemonade Stand Foundation for Childhood Cancer (n/a)

St. Baldrick's Foundation (n/a)
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Text and Data Mining valid from 2019-11-01

Text and Data Mining valid from 2019-11-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: Androgenetic chimerism as an etiology for Beckwith–Wiedemann syndrome: diagnosis and management

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0551-9

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics