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 & 50 others 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 journalComment/debate

Abstract

Corrections were made to the footnotes in Table 2.

Original languageEnglish (US)
Pages (from-to)764-765
Number of pages2
JournalGenetics in Medicine
Volume21
Issue number3
DOIs
StatePublished - Mar 1 2019

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Gene Deletion
Medicine
Phenotype

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

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

In: Genetics in Medicine, Vol. 21, No. 3, 01.03.2019, p. 764-765.

Research output: Contribution to journalComment/debate

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, Magdalena ; Callens, Tom ; Gomes, Alicia ; Sharp, Angela ; Chen, Yunjia ; Hicks, Alesha D. ; Aylsworth, Arthur S. ; Azizi, Amedeo A. ; Basel, Donald G. ; Bellus, Gary ; Bird, Lynne M. ; Blazo, Maria A. ; Burke, Leah W. ; Cannon, Ashley ; Collins, Felicity ; DeFilippo, Colette ; Denayer, Ellen ; Digilio, Maria C. ; Dills, Shelley K. ; Dosa, Laura ; Greenwood, Robert S. ; Griffis, Cristin ; Gupta, Punita ; Hachen, Rachel K. ; Hernández-Chico, Concepción ; Janssens, Sandra ; Jones, Kristi J. ; Jordan, Justin T. ; Kannu, Peter ; Korf, Bruce R. ; Lewis, Andrea M. ; Listernick, Robert H. ; Lonardo, Fortunato ; Mahoney, Maurice J. ; Ojeda, Mayra Martinez ; McDonald, Marie T. ; McDougall, Carey ; Mendelsohn, Nancy ; Miller, David T. ; Mori, Mari ; Oostenbrink, Rianne ; Perreault, Sebastién ; Pierpont, Mary Ella ; Piscopo, Carmelo ; Pond, Dinel A. ; Randolph, Linda M. ; Rauen, Katherine A. ; Rednam, Surya ; Rutledge, S. Lane ; Saletti, Veronica ; Schaefer, G. Bradley ; Schorry, Elizabeth K. ; Scott, Daryl A. ; Shugar, Andrea ; Siqveland, Elizabeth ; Starr, Lois J ; Syed, Ashraf ; Trapane, Pamela L. ; Ullrich, Nicole J. ; Wakefield, Emily G. ; Walsh, Laurence E. ; Wangler, Michael F. ; Zackai, Elaine ; Claes, Kathleen B.M. ; Wimmer, Katharina ; van Minkelen, Rick ; De Luca, Alessandro ; Martin, Yolanda ; Legius, Eric ; Messiaen, Ludwine M. / 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). In: Genetics in Medicine. 2019 ; Vol. 21, No. 3. pp. 764-765.
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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–phenotype correlation (Genetics in Medicine, (2018), 10.1038/s41436-018-0269-0)",
abstract = "Corrections were made to the footnotes in Table 2.",
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.}",
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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 - Corrections were made to the footnotes in Table 2.

AB - Corrections were made to the footnotes in Table 2.

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U2 - 10.1038/s41436-018-0326-8

DO - 10.1038/s41436-018-0326-8

M3 - Comment/debate

VL - 21

SP - 764

EP - 765

JO - Genetics in Medicine

JF - Genetics in Medicine

SN - 1098-3600

IS - 3

ER -