Correction to

The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3)

DDD Study

Research output: Contribution to journalComment/debate

Abstract

The article has been corrected to account for one patient being investigated through genome sequencing rather than exome sequencing as originally published; thus amendments to the Abstract and Methods have been made as well as addition of the relevant authors and acknowledgment.

Original languageEnglish
JournalGenetics in Medicine
DOIs
Publication statusPublished - Jan 1 2019

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Exome
Medicine
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ASJC Scopus subject areas

  • Genetics(clinical)

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@article{9866bbc6d1794f29b40107a22a2fd292,
title = "Correction to: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3)",
abstract = "The article has been corrected to account for one patient being investigated through genome sequencing rather than exome sequencing as originally published; thus amendments to the Abstract and Methods have been made as well as addition of the relevant authors and acknowledgment.",
author = "{DDD Study} and Juliette Piard and Lara Hawkes and Mathieu Milh and Laurent Villard and Renato Borgatti and Romina Romaniello and Melanie Fradin and Yline Capri and Delphine H{\'e}ron and Nougues, {Marie Christine} and Caroline Nava and Arsene, {Oana Tarta} and Debbie Shears and John Taylor and Alistair Pagnamenta and Taylor, {Jenny C.} and Yoshimi Sogawa and Diana Johnson and Helen Firth and Pradeep Vasudevan and Gabriela Jones and Nguyen-Morel, {Marie Ange} and Tiffany Busa and Agathe Roubertie and {van den Born}, Myrthe and Elise Brischoux-Boucher and Michel Koenig and Cyril Mignot and Usha Kini and Christophe Philippe",
year = "2019",
month = "1",
day = "1",
doi = "10.1038/s41436-019-0460-y",
language = "English",
journal = "Genetics in Medicine",
issn = "1098-3600",
publisher = "Nature Publishing Group",

}

TY - JOUR

T1 - Correction to

T2 - The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature (Genetics in Medicine, (2018), 10.1038/s41436-018-0339-3)

AU - DDD Study

AU - Piard, Juliette

AU - Hawkes, Lara

AU - Milh, Mathieu

AU - Villard, Laurent

AU - Borgatti, Renato

AU - Romaniello, Romina

AU - Fradin, Melanie

AU - Capri, Yline

AU - Héron, Delphine

AU - Nougues, Marie Christine

AU - Nava, Caroline

AU - Arsene, Oana Tarta

AU - Shears, Debbie

AU - Taylor, John

AU - Pagnamenta, Alistair

AU - Taylor, Jenny C.

AU - Sogawa, Yoshimi

AU - Johnson, Diana

AU - Firth, Helen

AU - Vasudevan, Pradeep

AU - Jones, Gabriela

AU - Nguyen-Morel, Marie Ange

AU - Busa, Tiffany

AU - Roubertie, Agathe

AU - van den Born, Myrthe

AU - Brischoux-Boucher, Elise

AU - Koenig, Michel

AU - Mignot, Cyril

AU - Kini, Usha

AU - Philippe, Christophe

PY - 2019/1/1

Y1 - 2019/1/1

N2 - The article has been corrected to account for one patient being investigated through genome sequencing rather than exome sequencing as originally published; thus amendments to the Abstract and Methods have been made as well as addition of the relevant authors and acknowledgment.

AB - The article has been corrected to account for one patient being investigated through genome sequencing rather than exome sequencing as originally published; thus amendments to the Abstract and Methods have been made as well as addition of the relevant authors and acknowledgment.

UR - http://www.scopus.com/inward/record.url?scp=85061972303&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85061972303&partnerID=8YFLogxK

U2 - 10.1038/s41436-019-0460-y

DO - 10.1038/s41436-019-0460-y

M3 - Comment/debate

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

ER -