Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)

Magdalena Koczkowska; Tom Callens; Alicia Gomes; Angela Sharp; Yunjia Chen; Alesha D. Hicks; Arthur S. Aylsworth; Amedeo A. Azizi; Donald G. Basel; Gary Bellus; Lynne M. Bird; Maria A. Blazo; Leah W. Burke; Ashley Cannon; Felicity Collins; Colette DeFilippo; Ellen Denayer; Maria C. Digilio; Shelley K. Dills; Laura Dosa; Robert S. Greenwood; Cristin Griffis; Punita Gupta; Rachel K. Hachen; Concepción Hernández-Chico; Sandra Janssens; Kristi J. Jones; Justin T. Jordan; Peter Kannu; Bruce R. Korf; Andrea M. Lewis; Robert H. Listernick; Fortunato Lonardo; Maurice J. Mahoney; Mayra Martinez Ojeda; Marie T. McDonald; Carey McDougall; Nancy Mendelsohn; David T. Miller; Mari Mori; Rianne Oostenbrink; Sebastién Perreault; Mary Ella Pierpont; Carmelo Piscopo; Dinel A. Pond; Linda M. Randolph; Katherine A. Rauen; Surya Rednam; S. Lane Rutledge; Veronica Saletti; G. Bradley Schaefer; Elizabeth K. Schorry; Daryl A. Scott; Andrea Shugar; Elizabeth Siqveland; Lois J. Starr; Ashraf Syed; Pamela L. Trapane; Nicole J. Ullrich; Emily G. Wakefield; Laurence E. Walsh; Michael F. Wangler; Elaine Zackai; Kathleen B.M. Claes; Katharina Wimmer; Rick van Minkelen; Alessandro De Luca; Yolanda Martin; Eric Legius; Ludwine M. Messiaen

doi:10.1038/s41436-018-0326-8

Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)

Magdalena Koczkowska
, Tom Callens
, Alicia Gomes
, Angela Sharp
, Yunjia Chen
, Alesha D. Hicks
, Arthur S. Aylsworth
, Amedeo A. Azizi
, Donald G. Basel
, Gary Bellus
, Lynne M. Bird
, Maria A. Blazo
, Leah W. Burke
, Ashley Cannon
, Felicity Collins
, Colette DeFilippo
, Ellen Denayer
, Maria C. Digilio
, Shelley K. Dills
, Laura Dosa

Robert S. Greenwood, Cristin Griffis, Punita Gupta, Rachel K. Hachen, Concepción Hernández-Chico, Sandra Janssens, Kristi J. Jones, Justin T. Jordan, Peter Kannu, Bruce R. Korf, Andrea M. Lewis, Robert H. Listernick, Fortunato Lonardo, Maurice J. Mahoney, Mayra Martinez Ojeda, Marie T. McDonald, Carey McDougall, Nancy Mendelsohn, David T. Miller, Mari Mori, Rianne Oostenbrink, Sebastién Perreault, Mary Ella Pierpont, Carmelo Piscopo, Dinel A. Pond, Linda M. Randolph, Katherine A. Rauen, Surya Rednam, S. Lane Rutledge, Veronica Saletti, G. Bradley Schaefer, Elizabeth K. Schorry, Daryl A. Scott, Andrea Shugar, Elizabeth Siqveland, Lois J. Starr, Ashraf Syed, Pamela L. Trapane, Nicole J. Ullrich, Emily G. Wakefield, Laurence E. Walsh, Michael F. Wangler, Elaine Zackai, Kathleen B.M. Claes, Katharina Wimmer, Rick van Minkelen, Alessandro De Luca, Yolanda Martin, Eric Legius, Ludwine M. Messiaen

Research output: Contribution to journal › Comment/debate › peer-review

2 Scopus citations

Abstract

A correction has been published to this Article. The PDF and HTML have been updated accordingly.

Original language	English (US)
Pages (from-to)	764-765
Number of pages	2
Journal	Genetics in Medicine
Volume	21
Issue number	3
DOIs	https://doi.org/10.1038/s41436-018-0326-8
State	Published - Mar 1 2019

Bibliographical note

Publisher Copyright:
© 2018, The Author(s).

PubMed: MeSH publication types

Published Erratum
Journal Article

Publisher link

10.1038/s41436-018-0326-8

Find It

Find It at U of M Libraries

Fingerprint

Dive into the research topics of 'Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)'. Together they form a unique fingerprint.

Cite this

Koczkowska, M., Callens, T., Gomes, A., Sharp, A., Chen, Y., Hicks, A. D., Aylsworth, A. S., Azizi, A. A., Basel, D. G., Bellus, G., Bird, L. M., Blazo, M. A., Burke, L. W., Cannon, A., Collins, F., DeFilippo, C., Denayer, E., Digilio, M. C., Dills, S. K., ... Messiaen, L. M. (2019). Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0). Genetics in Medicine, 21(3), 764-765. https://doi.org/10.1038/s41436-018-0326-8

Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0). / Koczkowska, Magdalena; Callens, Tom; Gomes, Alicia et al.
In: Genetics in Medicine, Vol. 21, No. 3, 01.03.2019, p. 764-765.

Research output: Contribution to journal › Comment/debate › peer-review

Koczkowska, M, Callens, T, Gomes, A, Sharp, A, Chen, Y, Hicks, AD, Aylsworth, AS, Azizi, AA, Basel, DG, Bellus, G, Bird, LM, Blazo, MA, Burke, LW, Cannon, A, Collins, F, DeFilippo, C, Denayer, E, Digilio, MC, Dills, SK, Dosa, L, Greenwood, RS, Griffis, C, Gupta, P, Hachen, RK, Hernández-Chico, C, Janssens, S, Jones, KJ, Jordan, JT, Kannu, P, Korf, BR, Lewis, AM, Listernick, RH, Lonardo, F, Mahoney, MJ, Ojeda, MM, McDonald, MT, McDougall, C, Mendelsohn, N, Miller, DT, Mori, M, Oostenbrink, R, Perreault, S, Pierpont, ME, Piscopo, C, Pond, DA, Randolph, LM, Rauen, KA, Rednam, S, Rutledge, SL, Saletti, V, Schaefer, GB, Schorry, EK, Scott, DA, Shugar, A, Siqveland, E, Starr, LJ, Syed, A, Trapane, PL, Ullrich, NJ, Wakefield, EG, Walsh, LE, Wangler, MF, Zackai, E, Claes, KBM, Wimmer, K, van Minkelen, R, De Luca, A, Martin, Y, Legius, E & Messiaen, LM 2019, 'Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)', Genetics in Medicine, vol. 21, no. 3, pp. 764-765. https://doi.org/10.1038/s41436-018-0326-8

Koczkowska M, Callens T, Gomes A, Sharp A, Chen Y, Hicks AD et al. Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0). Genetics in Medicine. 2019 Mar 1;21(3):764-765. doi: 10.1038/s41436-018-0326-8

@article{bacc6defd01546898ff2bf068edc494a,

title = "Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970\_2972del): an update of genotype{\textendash}phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)",

abstract = "A correction has been published to this Article. The PDF and HTML have been updated accordingly.",

author = "Magdalena Koczkowska and Tom Callens and Alicia Gomes and Angela Sharp and Yunjia Chen and Hicks, \{Alesha D.\} and Aylsworth, \{Arthur S.\} and Azizi, \{Amedeo A.\} and Basel, \{Donald G.\} and Gary Bellus and Bird, \{Lynne M.\} and Blazo, \{Maria A.\} and Burke, \{Leah W.\} and Ashley Cannon and Felicity Collins and Colette DeFilippo and Ellen Denayer and Digilio, \{Maria C.\} and Dills, \{Shelley K.\} and Laura Dosa and Greenwood, \{Robert S.\} and Cristin Griffis and Punita Gupta and Hachen, \{Rachel K.\} and Concepci{\'o}n Hern{\'a}ndez-Chico and Sandra Janssens and Jones, \{Kristi J.\} and Jordan, \{Justin T.\} and Peter Kannu and Korf, \{Bruce R.\} and Lewis, \{Andrea M.\} and Listernick, \{Robert H.\} and Fortunato Lonardo and Mahoney, \{Maurice J.\} and Ojeda, \{Mayra Martinez\} and McDonald, \{Marie T.\} and Carey McDougall and Nancy Mendelsohn and Miller, \{David T.\} and Mari Mori and Rianne Oostenbrink and Sebasti{\'e}n Perreault and Pierpont, \{Mary Ella\} and Carmelo Piscopo and Pond, \{Dinel A.\} and Randolph, \{Linda M.\} and Rauen, \{Katherine A.\} and Surya Rednam and Rutledge, \{S. Lane\} and Veronica Saletti and Schaefer, \{G. Bradley\} and Schorry, \{Elizabeth K.\} and Scott, \{Daryl A.\} and Andrea Shugar and Elizabeth Siqveland and Starr, \{Lois J.\} and Ashraf Syed and Trapane, \{Pamela L.\} and Ullrich, \{Nicole J.\} and Wakefield, \{Emily G.\} and Walsh, \{Laurence E.\} and Wangler, \{Michael F.\} and Elaine Zackai and Claes, \{Kathleen B.M.\} and Katharina Wimmer and \{van Minkelen\}, Rick and \{De Luca\}, Alessandro and Yolanda Martin and Eric Legius and Messiaen, \{Ludwine M.\}",

note = "Publisher Copyright: {\textcopyright} 2018, The Author(s).",

year = "2019",

month = mar,

day = "1",

doi = "10.1038/s41436-018-0326-8",

language = "English (US)",

volume = "21",

pages = "764--765",

journal = "Genetics in Medicine",

issn = "1098-3600",

publisher = "Elsevier B.V.",

number = "3",

}

TY - JOUR

T1 - Correction to

T2 - Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)

AU - Koczkowska, Magdalena

AU - Callens, Tom

AU - Gomes, Alicia

AU - Sharp, Angela

AU - Chen, Yunjia

AU - Hicks, Alesha D.

AU - Aylsworth, Arthur S.

AU - Azizi, Amedeo A.

AU - Basel, Donald G.

AU - Bellus, Gary

AU - Bird, Lynne M.

AU - Blazo, Maria A.

AU - Burke, Leah W.

AU - Cannon, Ashley

AU - Collins, Felicity

AU - DeFilippo, Colette

AU - Denayer, Ellen

AU - Digilio, Maria C.

AU - Dills, Shelley K.

AU - Dosa, Laura

AU - Greenwood, Robert S.

AU - Griffis, Cristin

AU - Gupta, Punita

AU - Hachen, Rachel K.

AU - Hernández-Chico, Concepción

AU - Janssens, Sandra

AU - Jones, Kristi J.

AU - Jordan, Justin T.

AU - Kannu, Peter

AU - Korf, Bruce R.

AU - Lewis, Andrea M.

AU - Listernick, Robert H.

AU - Lonardo, Fortunato

AU - Mahoney, Maurice J.

AU - Ojeda, Mayra Martinez

AU - McDonald, Marie T.

AU - McDougall, Carey

AU - Mendelsohn, Nancy

AU - Miller, David T.

AU - Mori, Mari

AU - Oostenbrink, Rianne

AU - Perreault, Sebastién

AU - Pierpont, Mary Ella

AU - Piscopo, Carmelo

AU - Pond, Dinel A.

AU - Randolph, Linda M.

AU - Rauen, Katherine A.

AU - Rednam, Surya

AU - Rutledge, S. Lane

AU - Saletti, Veronica

AU - Schaefer, G. Bradley

AU - Schorry, Elizabeth K.

AU - Scott, Daryl A.

AU - Shugar, Andrea

AU - Siqveland, Elizabeth

AU - Starr, Lois J.

AU - Syed, Ashraf

AU - Trapane, Pamela L.

AU - Ullrich, Nicole J.

AU - Wakefield, Emily G.

AU - Walsh, Laurence E.

AU - Wangler, Michael F.

AU - Zackai, Elaine

AU - Claes, Kathleen B.M.

AU - Wimmer, Katharina

AU - van Minkelen, Rick

AU - De Luca, Alessandro

AU - Martin, Yolanda

AU - Legius, Eric

AU - Messiaen, Ludwine M.

PY - 2019/3/1

Y1 - 2019/3/1

N2 - A correction has been published to this Article. The PDF and HTML have been updated accordingly.

AB - A correction has been published to this Article. The PDF and HTML have been updated accordingly.

UR - https://www.scopus.com/pages/publications/85054366647

UR - https://www.scopus.com/pages/publications/85054366647#tab=citedBy

U2 - 10.1038/s41436-018-0326-8

DO - 10.1038/s41436-018-0326-8

M3 - Comment/debate

C2 - 30275510

AN - SCOPUS:85054366647

SN - 1098-3600

VL - 21

SP - 764

EP - 765

JO - Genetics in Medicine

JF - Genetics in Medicine

IS - 3

ER -

Correction to: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)

Abstract

Bibliographical note

PubMed: MeSH publication types

Publisher link

Find It

Other files and links

Fingerprint

Cite this