P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome

Bibliographic Details
Main Authors: Stacey Cole, Brian Shayota, Vanina Taliercio, Brianna Stebbins, Gulsen Akay, Nicola Longo
Format: Article
Language:English
Published: Elsevier 2024-01-01
Series:Genetics in Medicine Open
Online Access:http://www.sciencedirect.com/science/article/pii/S2949774424003571
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author Stacey Cole
Brian Shayota
Vanina Taliercio
Brianna Stebbins
Gulsen Akay
Nicola Longo
author_facet Stacey Cole
Brian Shayota
Vanina Taliercio
Brianna Stebbins
Gulsen Akay
Nicola Longo
author_sort Stacey Cole
collection DOAJ
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institution Directory Open Access Journal
issn 2949-7744
language English
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publishDate 2024-01-01
publisher Elsevier
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series Genetics in Medicine Open
spelling doaj.art-d2e48e4133ee476f80a40f886e4e79b22024-03-09T09:31:38ZengElsevierGenetics in Medicine Open2949-77442024-01-012101211P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndromeStacey Cole0Brian Shayota1Vanina Taliercio2Brianna Stebbins3Gulsen Akay4Nicola Longo5University of UtahUniversity of UtahUniversity of UtahUniversity of UtahUniversity of UtahUniversity of Utahhttp://www.sciencedirect.com/science/article/pii/S2949774424003571
spellingShingle Stacey Cole
Brian Shayota
Vanina Taliercio
Brianna Stebbins
Gulsen Akay
Nicola Longo
P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
Genetics in Medicine Open
title P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
title_full P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
title_fullStr P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
title_full_unstemmed P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
title_short P317: Phenotypic variability among three family members with RAD21 Cornelia de Lange syndrome
title_sort p317 phenotypic variability among three family members with rad21 cornelia de lange syndrome
url http://www.sciencedirect.com/science/article/pii/S2949774424003571
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AT briannastebbins p317phenotypicvariabilityamongthreefamilymemberswithrad21corneliadelangesyndrome
AT gulsenakay p317phenotypicvariabilityamongthreefamilymemberswithrad21corneliadelangesyndrome
AT nicolalongo p317phenotypicvariabilityamongthreefamilymemberswithrad21corneliadelangesyndrome