Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)

Karin Weiss; Hayley P. Lazar; Alina Kurolap; Ariel F. Martinez; Tamar Paperna; Lior Cohen; Marie F. Smeland; Sandra Whalen; Solveig Heide; Boris Keren; Pauline Terhal; Melita Irving; Motoki Takaku; John D. Roberts; Robert M. Petrovich; Samantha A.Schrier Vergano; Amy Kenney; Hanne Hove; Elizabeth DeChene; Shane C. Quinonez; Estelle Colin; Alban Ziegler; Melissa Rumple; Mahim Jain; Danielle Monteil; Elizabeth R. Roeder; Kimberly Nugent; Arie van Haeringen; Michael Gambello; Avni Santani; Līvija Medne; Bryan Krock; Cara M. Skraban; Elaine H. Zackai; Holly A. Dubbs; Thomas Smol; Jamal Ghoumid; Michael J. Parker; Michael Wright; Peter Turnpenny; Jill Clayton-Smith; Kay Metcalfe; Hitoshi Kurumizaka; Bruce D. Gelb; Hagit Baris Feldman; Philippe M. Campeau; Maximilian Muenke; Paul A. Wade; Katherine Lachlan

doi:10.1038/s41436-019-0727-3

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)

Karin Weiss
, Hayley P. Lazar
, Alina Kurolap
, Ariel F. Martinez
, Tamar Paperna
, Lior Cohen
, Marie F. Smeland
, Sandra Whalen
, Solveig Heide
, Boris Keren
, Pauline Terhal
, Melita Irving
, Motoki Takaku
, John D. Roberts
, Robert M. Petrovich
, Samantha A.Schrier Vergano
, Amy Kenney
, Hanne Hove
, Elizabeth DeChene
, Shane C. Quinonez

Estelle Colin, Alban Ziegler, Melissa Rumple, Mahim Jain, Danielle Monteil, Elizabeth R. Roeder, Kimberly Nugent, Arie van Haeringen, Michael Gambello, Avni Santani, Līvija Medne, Bryan Krock, Cara M. Skraban, Elaine H. Zackai, Holly A. Dubbs, Thomas Smol, Jamal Ghoumid, Michael J. Parker, Michael Wright, Peter Turnpenny, Jill Clayton-Smith, Kay Metcalfe, Hitoshi Kurumizaka, Bruce D. Gelb, Hagit Baris Feldman, Philippe M. Campeau, Maximilian Muenke, Paul A. Wade, Katherine Lachlan

Rambam Health Care Campus
National Institutes of Health
Technion-Israel Institute of Technology
Tel Aviv University
University Hospital of North Norway
Pierre and Marie Curie University
Sorbonne Université
Utrecht University
King's College London
Hospital of the King's Daughters
Eastern Virginia Medical School
University of Copenhagen
The Children's Hospital of Philadelphia
University of Michigan, Ann Arbor
Université d'Angers
Banner Children's Specialists Neurology Clinic
Medical Genetics Branch
Bone and Osteogenesis Imperfecta Department
Kennedy Krieger Institute
Naval Medical Center - Portsmouth
Baylor College of Medicine
Leiden University
Emory University
Université de Lille
Sheffield Children's NHS Foundation Trust
Newcastle upon Tyne Hospitals NHS Foundation Trust
University of Exeter
University of Manchester
Manchester University NHS Foundation Trust
Waseda University
Icahn School of Medicine at Mount Sinai
University of Montreal
University Hospital Southampton NHS Foundation Trust

Research output: Contribution to journal › Comment/debate

6 Scopus citations

Abstract

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Original language	English
Pages (from-to)	669
Number of pages	1
Journal	Genetics in Medicine
Volume	22
Issue number	3
DOIs	https://doi.org/10.1038/s41436-019-0727-3
State	Published - 1 Mar 2020
Externally published	Yes

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Weiss, K., Lazar, H. P., Kurolap, A., Martinez, A. F., Paperna, T., Cohen, L., Smeland, M. F., Whalen, S., Heide, S., Keren, B., Terhal, P., Irving, M., Takaku, M., Roberts, J. D., Petrovich, R. M., Vergano, S. A. S., Kenney, A., Hove, H., DeChene, E., ... Lachlan, K. (2020). Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0). Genetics in Medicine, 22(3), 669. https://doi.org/10.1038/s41436-019-0727-3

@article{2d6c2e1b2e5f4b46a05ca2b8507690ad,

title = "Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype{\textendash}phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)",

abstract = "An amendment to this paper has been published and can be accessed via a link at the top of the paper.",

author = "Karin Weiss and Lazar, \{Hayley P.\} and Alina Kurolap and Martinez, \{Ariel F.\} and Tamar Paperna and Lior Cohen and Smeland, \{Marie F.\} and Sandra Whalen and Solveig Heide and Boris Keren and Pauline Terhal and Melita Irving and Motoki Takaku and Roberts, \{John D.\} and Petrovich, \{Robert M.\} and Vergano, \{Samantha A.Schrier\} and Amy Kenney and Hanne Hove and Elizabeth DeChene and Quinonez, \{Shane C.\} and Estelle Colin and Alban Ziegler and Melissa Rumple and Mahim Jain and Danielle Monteil and Roeder, \{Elizabeth R.\} and Kimberly Nugent and \{van Haeringen\}, Arie and Michael Gambello and Avni Santani and Līvija Medne and Bryan Krock and Skraban, \{Cara M.\} and Zackai, \{Elaine H.\} and Dubbs, \{Holly A.\} and Thomas Smol and Jamal Ghoumid and Parker, \{Michael J.\} and Michael Wright and Peter Turnpenny and Jill Clayton-Smith and Kay Metcalfe and Hitoshi Kurumizaka and Gelb, \{Bruce D.\} and Feldman, \{Hagit Baris\} and Campeau, \{Philippe M.\} and Maximilian Muenke and Wade, \{Paul A.\} and Katherine Lachlan",

note = "Publisher Copyright: {\textcopyright} 2019, American College of Medical Genetics and Genomics.",

year = "2020",

month = mar,

day = "1",

doi = "10.1038/s41436-019-0727-3",

language = "English",

volume = "22",

pages = "669",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier B.V.",

number = "3",

}

Weiss, K, Lazar, HP, Kurolap, A, Martinez, AF, Paperna, T, Cohen, L, Smeland, MF, Whalen, S, Heide, S, Keren, B, Terhal, P, Irving, M, Takaku, M, Roberts, JD, Petrovich, RM, Vergano, SAS, Kenney, A, Hove, H, DeChene, E, Quinonez, SC, Colin, E, Ziegler, A, Rumple, M, Jain, M, Monteil, D, Roeder, ER, Nugent, K, van Haeringen, A, Gambello, M, Santani, A, Medne, L, Krock, B, Skraban, CM, Zackai, EH, Dubbs, HA, Smol, T, Ghoumid, J, Parker, MJ, Wright, M, Turnpenny, P, Clayton-Smith, J, Metcalfe, K, Kurumizaka, H, Gelb, BD, Feldman, HB, Campeau, PM, Muenke, M, Wade, PA & Lachlan, K 2020, 'Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)', Genetics in Medicine, vol. 22, no. 3, pp. 669. https://doi.org/10.1038/s41436-019-0727-3

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0). / Weiss, Karin; Lazar, Hayley P.; Kurolap, Alina et al.
In: Genetics in Medicine, Vol. 22, No. 3, 01.03.2020, p. 669.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Correction

T2 - The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)

AU - Weiss, Karin

AU - Lazar, Hayley P.

AU - Kurolap, Alina

AU - Martinez, Ariel F.

AU - Paperna, Tamar

AU - Cohen, Lior

AU - Smeland, Marie F.

AU - Whalen, Sandra

AU - Heide, Solveig

AU - Keren, Boris

AU - Terhal, Pauline

AU - Irving, Melita

AU - Takaku, Motoki

AU - Roberts, John D.

AU - Petrovich, Robert M.

AU - Vergano, Samantha A.Schrier

AU - Kenney, Amy

AU - Hove, Hanne

AU - DeChene, Elizabeth

AU - Quinonez, Shane C.

AU - Colin, Estelle

AU - Ziegler, Alban

AU - Rumple, Melissa

AU - Jain, Mahim

AU - Monteil, Danielle

AU - Roeder, Elizabeth R.

AU - Nugent, Kimberly

AU - van Haeringen, Arie

AU - Gambello, Michael

AU - Santani, Avni

AU - Medne, Līvija

AU - Krock, Bryan

AU - Skraban, Cara M.

AU - Zackai, Elaine H.

AU - Dubbs, Holly A.

AU - Smol, Thomas

AU - Ghoumid, Jamal

AU - Parker, Michael J.

AU - Wright, Michael

AU - Turnpenny, Peter

AU - Clayton-Smith, Jill

AU - Metcalfe, Kay

AU - Kurumizaka, Hitoshi

AU - Gelb, Bruce D.

AU - Feldman, Hagit Baris

AU - Campeau, Philippe M.

AU - Muenke, Maximilian

AU - Wade, Paul A.

AU - Lachlan, Katherine

PY - 2020/3/1

Y1 - 2020/3/1

N2 - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

AB - An amendment to this paper has been published and can be accessed via a link at the top of the paper.

UR - https://www.scopus.com/pages/publications/85081090678

U2 - 10.1038/s41436-019-0727-3

DO - 10.1038/s41436-019-0727-3

M3 - Comment/debate

C2 - 31844176

AN - SCOPUS:85081090678

SN - 1098-3600

VL - 22

SP - 669

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 3

ER -

Weiss K, Lazar HP, Kurolap A, Martinez AF, Paperna T, Cohen L et al. Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0). Genetics in Medicine. 2020 Mar 1;22(3):669. doi: 10.1038/s41436-019-0727-3

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis (Genetics in Medicine, (2020), 22, 2, (389-397), 10.1038/s41436-019-0612-0)

Abstract

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