Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

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

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. QuinonezEstelle 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

^*Corresponding author for this work

Research output: Contribution to journal › Comment/Letter to the editor › Academic › peer-review

Abstract

Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019

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
Publication status	Published - Mar 2020

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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, 22(3), 669. https://doi.org/10.1038/s41436-019-0727-3

@article{d6e399001ccd4e8c971d4df20f648784,

title = "Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis",

abstract = "Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019",

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",

year = "2020",

month = mar,

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

language = "English",

volume = "22",

pages = "669",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Lippincott Williams & Wilkins",

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, vol. 22, no. 3, pp. 669. https://doi.org/10.1038/s41436-019-0727-3

TY - JOUR

T1 - Correction

T2 - The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

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

Y1 - 2020/3

N2 - Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019

AB - Correction to: Genetics in Medicine 2019; https://doi.org/10.1038/s41436-019-0612-0; published online 07 August 2019

UR - http://www.scopus.com/inward/record.url?scp=85081090678&partnerID=8YFLogxK

U2 - 10.1038/s41436-019-0727-3

DO - 10.1038/s41436-019-0727-3

M3 - Comment/Letter to the editor

C2 - 31844176

AN - SCOPUS:85081090678

SN - 1098-3600

VL - 22

SP - 669

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 3

ER -

Correction: The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype-phenotype correlations, and molecular basis

Abstract

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