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Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature

Crossref DOI link: https://doi.org/10.1038/s41436-019-0454-9

Published Print: 2019-09

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

Authors

Torti, Erin http://orcid.org/0000-0001-5790-1051
Keren, Boris

Palmer, Elizabeth E.

Zhu, Zehua

Afenjar, Alexandra

Anderson, Ilse. J.

Andrews, Marisa V.

Atkinson, Celia

Au, Margaret

Berry, Susan A.

Bowling, Kevin M.

Boyle, Jackie

Buratti, Julien

Cathey, Sara S.

Charles, Perrine

Cogne, Benjamin

Courtin, Thomas

Escobar, Luis F.

Finley, Sabra Ledare

Graham, John M. Jr.

Grange, Dorothy K.

Heron, Delphine

Hewson, Stacy

Hiatt, Susan M.

Hibbs, Kathleen A.

Jayakar, Parul

Kalsner, Louisa

Larcher, Lise

Lesca, Gaetan

Mark, Paul R.

Miller, Kathryn

Nava, Caroline

Nizon, Mathilde

Pai, G. Shashidhar

Pappas, John

Parsons, Gretchen

Payne, Katelyn

Putoux, Audrey

Rabin, Rachel

Sabatier, Isabelle

Shinawi, Marwan

Shur, Natasha

Skinner, Steven A.

Valence, Stephanie

Warren, Hannah

Whalen, Sandra

Crunk, Amy

Douglas, Ganka

Monaghan, Kristin G.

Person, Richard E.

Willaert, Rebecca

Solomon, Benjamin D.

Juusola, Jane
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Text and Data Mining valid from 2019-09-01

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

Article Title: Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0454-9

Content Type: article

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

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