Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)

C. M. Clarke; V. T. Fok; J. A. Gustafson; M. D. Smyth; A. E. Timms; C. D. Frazar; J. D. Smith; C. B. Birgfeld; A. Lee; R. G. Ellenbogen; J. S. Gruss; R. A. Hopper; M. L. Cunningham

doi:10.1002/ajmg.a.38846

Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)

C. M. Clarke
, V. T. Fok
, J. A. Gustafson
, M. D. Smyth
, A. E. Timms
, C. D. Frazar
, J. D. Smith
, C. B. Birgfeld
, A. Lee
, R. G. Ellenbogen
, J. S. Gruss
, R. A. Hopper
, M. L. Cunningham

Department of Neurosurgery

Research output: Contribution to journal › Comment/debate

4 Scopus citations

Abstract

DOI: 10.1002/ajmg.a.38540 After publishing this manuscript two data errors were identified. Neither error affects the interpretation of the data. Table 3 lists three patients with TCF12 variants. Proband 95628 is listed as a female with a c.1907A>G; p.(Lys636Arg) variant. This proband is male, not female. This proband is correctly listed as a male in Supplemental Table S1a. Table 4 and Supplemental Table S1b list four probands with SCARF2 variants. Proband 95585 is inaccurately listed as having c.2593dupG: p.Ala865Serfs*184. The correct variant designation is c.2596dupG: p.Ala866Glyfs*191.

Original language	English
Pages (from-to)	2522
Number of pages	1
Journal	American Journal of Medical Genetics, Part A
Volume	176
Issue number	11
DOIs	https://doi.org/10.1002/ajmg.a.38846
State	Published - Nov 2018

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Clarke, C. M., Fok, V. T., Gustafson, J. A., Smyth, M. D., Timms, A. E., Frazar, C. D., Smith, J. D., Birgfeld, C. B., Lee, A., Ellenbogen, R. G., Gruss, J. S., Hopper, R. A., & Cunningham, M. L. (2018). Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540). American Journal of Medical Genetics, Part A, 176(11), 2522. https://doi.org/10.1002/ajmg.a.38846

@article{aeac1d3704d0497ba1a837da3a08c6e2,

title = "Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)",

abstract = "DOI: 10.1002/ajmg.a.38540 After publishing this manuscript two data errors were identified. Neither error affects the interpretation of the data. Table 3 lists three patients with TCF12 variants. Proband 95628 is listed as a female with a c.1907A>G; p.(Lys636Arg) variant. This proband is male, not female. This proband is correctly listed as a male in Supplemental Table S1a. Table 4 and Supplemental Table S1b list four probands with SCARF2 variants. Proband 95585 is inaccurately listed as having c.2593dupG: p.Ala865Serfs*184. The correct variant designation is c.2596dupG: p.Ala866Glyfs*191.",

author = "Clarke, \{C. M.\} and Fok, \{V. T.\} and Gustafson, \{J. A.\} and Smyth, \{M. D.\} and Timms, \{A. E.\} and Frazar, \{C. D.\} and Smith, \{J. D.\} and Birgfeld, \{C. B.\} and A. Lee and Ellenbogen, \{R. G.\} and Gruss, \{J. S.\} and Hopper, \{R. A.\} and Cunningham, \{M. L.\}",

note = "Publisher Copyright: {\textcopyright} 2018 Wiley Periodicals, Inc.",

year = "2018",

month = nov,

doi = "10.1002/ajmg.a.38846",

language = "English",

volume = "176",

pages = "2522",

journal = "American Journal of Medical Genetics, Part A",

issn = "1552-4825",

number = "11",

}

Clarke, CM, Fok, VT, Gustafson, JA, Smyth, MD, Timms, AE, Frazar, CD, Smith, JD, Birgfeld, CB, Lee, A, Ellenbogen, RG, Gruss, JS, Hopper, RA & Cunningham, ML 2018, 'Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)', American Journal of Medical Genetics, Part A, vol. 176, no. 11, pp. 2522. https://doi.org/10.1002/ajmg.a.38846

Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540). / Clarke, C. M.; Fok, V. T.; Gustafson, J. A. et al.
In: American Journal of Medical Genetics, Part A, Vol. 176, No. 11, 11.2018, p. 2522.

Research output: Contribution to journal › Comment/debate

TY - JOUR

T1 - Corrigendum to

T2 - Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)

AU - Clarke, C. M.

AU - Fok, V. T.

AU - Gustafson, J. A.

AU - Smyth, M. D.

AU - Timms, A. E.

AU - Frazar, C. D.

AU - Smith, J. D.

AU - Birgfeld, C. B.

AU - Lee, A.

AU - Ellenbogen, R. G.

AU - Gruss, J. S.

AU - Hopper, R. A.

AU - Cunningham, M. L.

PY - 2018/11

Y1 - 2018/11

N2 - DOI: 10.1002/ajmg.a.38540 After publishing this manuscript two data errors were identified. Neither error affects the interpretation of the data. Table 3 lists three patients with TCF12 variants. Proband 95628 is listed as a female with a c.1907A>G; p.(Lys636Arg) variant. This proband is male, not female. This proband is correctly listed as a male in Supplemental Table S1a. Table 4 and Supplemental Table S1b list four probands with SCARF2 variants. Proband 95585 is inaccurately listed as having c.2593dupG: p.Ala865Serfs*184. The correct variant designation is c.2596dupG: p.Ala866Glyfs*191.

AB - DOI: 10.1002/ajmg.a.38540 After publishing this manuscript two data errors were identified. Neither error affects the interpretation of the data. Table 3 lists three patients with TCF12 variants. Proband 95628 is listed as a female with a c.1907A>G; p.(Lys636Arg) variant. This proband is male, not female. This proband is correctly listed as a male in Supplemental Table S1a. Table 4 and Supplemental Table S1b list four probands with SCARF2 variants. Proband 95585 is inaccurately listed as having c.2593dupG: p.Ala865Serfs*184. The correct variant designation is c.2596dupG: p.Ala866Glyfs*191.

UR - https://www.scopus.com/pages/publications/85053521198

U2 - 10.1002/ajmg.a.38846

DO - 10.1002/ajmg.a.38846

M3 - Comment/debate

C2 - 30537273

AN - SCOPUS:85053521198

SN - 1552-4825

VL - 176

SP - 2522

JO - American Journal of Medical Genetics, Part A

JF - American Journal of Medical Genetics, Part A

IS - 11

ER -

Clarke CM, Fok VT, Gustafson JA, Smyth MD, Timms AE, Frazar CD et al. Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540). American Journal of Medical Genetics, Part A. 2018 Nov;176(11):2522. doi: 10.1002/ajmg.a.38846

Corrigendum to: Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms (American Journal of Medical Genetics Part A, (2018), 176, 2, (290-300), 10.1002/ajmg.a.38540)

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