Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

Francesco Vetrini; Shane McKee; Jill A. Rosenfeld; Mohnish Suri; Andrea M. Lewis; Kimberly Margaret Nugent; Elizabeth Roeder; Rebecca O. Littlejohn; Sue Holder; Wenmiao Zhu; Joseph T. Alaimo; Brett Graham; Jill M. Harris; James B. Gibson; Matthew Pastore; Kim L. McBride; Makanko Komara; Lihadh Al-Gazali; Aisha Al Shamsi; Elizabeth A. Fanning; Klaas J. Wierenga; Daryl A. Scott; Ziva Ben-Neriah; Vardiella Meiner; Hanoch Cassuto; Orly Elpeleg; J. Lloyd Holder; Lindsay C. Burrage; Laurie H. Seaver; Lionel Van Maldergem; Sonal Mahida; Janet S. Soul; Margaret Marlatt; Ludmila Matyakhina; Julie Vogt; June Anne Gold; Soo Mi Park; Vinod Varghese; Anne K. Lampe; Ajith Kumar; Melissa Lees; Muriel Holder-Espinasse; Vivienne McConnell; Birgitta Bernhard; Ed Blair; Victoria Harrison; Donna M. Muzny; Richard A. Gibbs; Sarah H. Elsea; Jennifer E. Posey; Weimin Bi; Seema Lalani; Fan Xia; Yaping Yang; Christine M. Eng; James R. Lupski; Pengfei Liu

doi:10.1186/s13073-019-0630-1

Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

Francesco Vetrini, Shane McKee, Jill A. Rosenfeld, Mohnish Suri, Andrea M. Lewis, Kimberly Margaret Nugent, Elizabeth Roeder, Rebecca O. Littlejohn, Sue Holder, Wenmiao Zhu, Joseph T. Alaimo, Brett Graham, Jill M. Harris, James B. Gibson, Matthew Pastore, Kim L. McBride, Makanko Komara, Lihadh Al-Gazali, Aisha Al Shamsi, Elizabeth A. FanningKlaas J. Wierenga, Daryl A. Scott, Ziva Ben-Neriah, Vardiella Meiner, Hanoch Cassuto, Orly Elpeleg, J. Lloyd Holder, Lindsay C. Burrage, Laurie H. Seaver, Lionel Van Maldergem, Sonal Mahida, Janet S. Soul, Margaret Marlatt, Ludmila Matyakhina, Julie Vogt, June Anne Gold, Soo Mi Park, Vinod Varghese, Anne K. Lampe, Ajith Kumar, Melissa Lees, Muriel Holder-Espinasse, Vivienne McConnell, Birgitta Bernhard, Ed Blair, Victoria Harrison, Donna M. Muzny, Richard A. Gibbs, Sarah H. Elsea, Jennifer E. Posey, Weimin Bi, Seema Lalani, Fan Xia, Yaping Yang, Christine M. Eng, James R. Lupski, Pengfei Liu

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

Original language	English
Article number	16
Journal	Genome Medicine
Volume	11
Issue number	1
DOIs	https://doi.org/10.1186/s13073-019-0630-1
State	Published - Mar 25 2019

ASJC Scopus Subject Areas

Molecular Medicine
Molecular Biology
Genetics
Genetics(clinical)

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Vetrini, F., McKee, S., Rosenfeld, J. A., Suri, M., Lewis, A. M., Nugent, K. M., Roeder, E., Littlejohn, R. O., Holder, S., Zhu, W., Alaimo, J. T., Graham, B., Harris, J. M., Gibson, J. B., Pastore, M., McBride, K. L., Komara, M., Al-Gazali, L., Al Shamsi, A., ... Liu, P. (2019). Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). Genome Medicine, 11(1), Article 16. https://doi.org/10.1186/s13073-019-0630-1

Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). / Vetrini, Francesco; McKee, Shane; Rosenfeld, Jill A. et al.
In: Genome Medicine, Vol. 11, No. 1, 16, 25.03.2019.

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

Vetrini, F, McKee, S, Rosenfeld, JA, Suri, M, Lewis, AM, Nugent, KM, Roeder, E, Littlejohn, RO, Holder, S, Zhu, W, Alaimo, JT, Graham, B, Harris, JM, Gibson, JB, Pastore, M, McBride, KL, Komara, M, Al-Gazali, L, Al Shamsi, A, Fanning, EA, Wierenga, KJ, Scott, DA, Ben-Neriah, Z, Meiner, V, Cassuto, H, Elpeleg, O, Lloyd Holder, J, Burrage, LC, Seaver, LH, Van Maldergem, L, Mahida, S, Soul, JS, Marlatt, M, Matyakhina, L, Vogt, J, Gold, JA, Park, SM, Varghese, V, Lampe, AK, Kumar, A, Lees, M, Holder-Espinasse, M, McConnell, V, Bernhard, B, Blair, E, Harrison, V, Muzny, DM, Gibbs, RA, Elsea, SH, Posey, JE, Bi, W, Lalani, S, Xia, F, Yang, Y, Eng, CM, Lupski, JR & Liu, P 2019, 'Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)', Genome Medicine, vol. 11, no. 1, 16. https://doi.org/10.1186/s13073-019-0630-1

Vetrini F, McKee S, Rosenfeld JA, Suri M, Lewis AM, Nugent KM et al. Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). Genome Medicine. 2019 Mar 25;11(1):16. doi: 10.1186/s13073-019-0630-1

Vetrini, Francesco ; McKee, Shane ; Rosenfeld, Jill A. et al. / Correction : De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0). In: Genome Medicine. 2019 ; Vol. 11, No. 1.

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AU - McKee, Shane

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AU - Suri, Mohnish

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AU - Nugent, Kimberly Margaret

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AU - Littlejohn, Rebecca O.

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AU - Al Shamsi, Aisha

AU - Fanning, Elizabeth A.

AU - Wierenga, Klaas J.

AU - Scott, Daryl A.

AU - Ben-Neriah, Ziva

AU - Meiner, Vardiella

AU - Cassuto, Hanoch

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AU - Mahida, Sonal

AU - Soul, Janet S.

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AU - Matyakhina, Ludmila

AU - Vogt, Julie

AU - Gold, June Anne

AU - Park, Soo Mi

AU - Varghese, Vinod

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AU - Kumar, Ajith

AU - Lees, Melissa

AU - Holder-Espinasse, Muriel

AU - McConnell, Vivienne

AU - Bernhard, Birgitta

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AU - Harrison, Victoria

AU - Muzny, Donna M.

AU - Gibbs, Richard A.

AU - Elsea, Sarah H.

AU - Posey, Jennifer E.

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Correction: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndrome (Genome Medicine (2019) 11 (12) DOI: 10.1186/s13073-019-0623-0)

ASJC Scopus Subject Areas

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