Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)

Genomics England Research Consortium

doi:10.1038/s41436-020-0784-7

Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)

Genomics England Research Consortium

Genomics England
University of Manchester
University of Leeds
Leeds Teaching Hospitals NHS Trust
Liverpool Women's NHS Foundation Trust
Northwick Park Hospital
Universidad de Chile
Guy's and St Thomas' NHS Foundation Trust
Children's University Hospital Dublin
Wellcome Trust Sanger Institute
University of Bologna
St George's University of London
King's College London
IRCCS Ospedale Casa Sollievo della Sofferenza - San Giovanni Rotondo (FG)
Queen Mary University of London
Royal Manchester Children’s Hospital
Royal Devon & Exeter NHS Foundation Trust
University of Exeter
Manchester University NHS Foundation Trust

Research output: Contribution to journal › Comment/debate

2 Scopus citations

Abstract

Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.

Original language	English
Pages (from-to)	980
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	5
DOIs	https://doi.org/10.1038/s41436-020-0784-7
State	Published - 1 May 2020

Access to Document

10.1038/s41436-020-0784-7

Fingerprint

Dive into the research topics of 'Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)'. Together they form a unique fingerprint.

Cite this

@article{de6651bf18ed4f9a83136ddc67fe3f34,

title = "Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)",

abstract = "Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.",

author = "\{Genomics England Research Consortium\} and Sara Cuvertino and Verity Hartill and Alice Colyer and Terence Garner and Nisha Nair and Lihadh Al-Gazali and Natalie Canham and Victor Faundes and Frances Flinter and Jozef Hertecant and Muriel Holder-Espinasse and Brian Jackson and Lynch, \{Sally Ann\} and Fatima Nadat and Narasimhan, \{Vagheesh M.\} and Michelle Peckham and Robert Sellers and Marco Seri and Francesca Montanari and Laura Southgate and Squeo, \{Gabriella Maria\} and Richard Trembath and \{van Heel\}, David and Santina Venuto and Daniel Weisberg and Karen Stals and Sian Ellard and Anne Barton and Kimber, \{Susan J.\} and Eamonn Sheridan and Giuseppe Merla and Adam Stevens and Johnson, \{Colin A.\} and Siddharth Banka",

note = "Publisher Copyright: {\textcopyright} 2020, The Author(s).",

year = "2020",

month = may,

day = "1",

doi = "10.1038/s41436-020-0784-7",

language = "English",

volume = "22",

pages = "980",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier BV",

number = "5",

}

TY - JOUR

T1 - Correction

T2 - A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)

AU - Genomics England Research Consortium

AU - Cuvertino, Sara

AU - Hartill, Verity

AU - Colyer, Alice

AU - Garner, Terence

AU - Nair, Nisha

AU - Al-Gazali, Lihadh

AU - Canham, Natalie

AU - Faundes, Victor

AU - Flinter, Frances

AU - Hertecant, Jozef

AU - Holder-Espinasse, Muriel

AU - Jackson, Brian

AU - Lynch, Sally Ann

AU - Nadat, Fatima

AU - Narasimhan, Vagheesh M.

AU - Peckham, Michelle

AU - Sellers, Robert

AU - Seri, Marco

AU - Montanari, Francesca

AU - Southgate, Laura

AU - Squeo, Gabriella Maria

AU - Trembath, Richard

AU - van Heel, David

AU - Venuto, Santina

AU - Weisberg, Daniel

AU - Stals, Karen

AU - Ellard, Sian

AU - Barton, Anne

AU - Kimber, Susan J.

AU - Sheridan, Eamonn

AU - Merla, Giuseppe

AU - Stevens, Adam

AU - Johnson, Colin A.

AU - Banka, Siddharth

PY - 2020/5/1

Y1 - 2020/5/1

N2 - Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.

AB - Correction to: Genetics in Medicine 22:2020 https://doi.org/10.1038/s41436-019-0743-3 published online 17 January 2020. An incorrect reference was cited in the fourth sentence of the Results section. The correct citation should have been Al-Gazali LI, Hamid Z, Hertecant J et al. An autosomal recessive syndrome of choanal atresia, hypothelia/athelia and thyroid gland anomalies overlapping Bamforth syndrome, ANOTHER syndrome and methimazole embryopathy. Clin Dysmorphol 2002;2:79–85. This has now been corrected in both the PDF and HTML versions of the Article.

UR - https://www.scopus.com/pages/publications/85082190394

U2 - 10.1038/s41436-020-0784-7

DO - 10.1038/s41436-020-0784-7

M3 - Comment/debate

C2 - 32203228

AN - SCOPUS:85082190394

SN - 1098-3600

VL - 22

SP - 980

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 5

ER -

Correction: A restricted spectrum of missense KMT2D variants cause a multiple malformations disorder distinct from Kabuki syndrome (Genetics in Medicine, (2020), 22, 5, (867-877), 10.1038/s41436-019-0743-3)

Abstract

Access to Document

Other files and links

Fingerprint

Cite this