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Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434874/ https://www.ncbi.nlm.nih.gov/pubmed/30909959 http://dx.doi.org/10.1186/s13073-019-0630-1 |
| _version_ | 1783406559907282944 |
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| author | Vetrini, Francesco McKee, Shane Rosenfeld, Jill A. Suri, Mohnish Lewis, Andrea M. Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O. Holder, Sue Zhu, Wenmiao Alaimo, Joseph T. Graham, Brett Harris, Jill M. Gibson, James B. Pastore, Matthew McBride, Kim L. Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A. Wierenga, Klaas J. Scott, Daryl A. Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Lloyd Holder Jr, J. Burrage, Lindsay C. Seaver, Laurie H. Van Maldergem, Lionel Mahida, Sonal Soul, Janet S. Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K. Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M. Gibbs, Richard A. Elsea, Sarah H. Posey, Jennifer E. Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M. Lupski, James R. Liu, Pengfei |
| author_facet | Vetrini, Francesco McKee, Shane Rosenfeld, Jill A. Suri, Mohnish Lewis, Andrea M. Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O. Holder, Sue Zhu, Wenmiao Alaimo, Joseph T. Graham, Brett Harris, Jill M. Gibson, James B. Pastore, Matthew McBride, Kim L. Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A. Wierenga, Klaas J. Scott, Daryl A. Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Lloyd Holder Jr, J. Burrage, Lindsay C. Seaver, Laurie H. Van Maldergem, Lionel Mahida, Sonal Soul, Janet S. Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K. Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M. Gibbs, Richard A. Elsea, Sarah H. Posey, Jennifer E. Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M. Lupski, James R. Liu, Pengfei |
| author_sort | Vetrini, Francesco |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6434874 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-64348742019-04-08 Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome Vetrini, Francesco McKee, Shane Rosenfeld, Jill A. Suri, Mohnish Lewis, Andrea M. Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O. Holder, Sue Zhu, Wenmiao Alaimo, Joseph T. Graham, Brett Harris, Jill M. Gibson, James B. Pastore, Matthew McBride, Kim L. Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A. Wierenga, Klaas J. Scott, Daryl A. Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Lloyd Holder Jr, J. Burrage, Lindsay C. Seaver, Laurie H. Van Maldergem, Lionel Mahida, Sonal Soul, Janet S. Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K. Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M. Gibbs, Richard A. Elsea, Sarah H. Posey, Jennifer E. Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M. Lupski, James R. Liu, Pengfei Genome Med Correction BioMed Central 2019-03-25 /pmc/articles/PMC6434874/ /pubmed/30909959 http://dx.doi.org/10.1186/s13073-019-0630-1 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
| spellingShingle | Correction Vetrini, Francesco McKee, Shane Rosenfeld, Jill A. Suri, Mohnish Lewis, Andrea M. Nugent, Kimberly Margaret Roeder, Elizabeth Littlejohn, Rebecca O. Holder, Sue Zhu, Wenmiao Alaimo, Joseph T. Graham, Brett Harris, Jill M. Gibson, James B. Pastore, Matthew McBride, Kim L. Komara, Makanko Al-Gazali, Lihadh Al Shamsi, Aisha Fanning, Elizabeth A. Wierenga, Klaas J. Scott, Daryl A. Ben-Neriah, Ziva Meiner, Vardiella Cassuto, Hanoch Elpeleg, Orly Lloyd Holder Jr, J. Burrage, Lindsay C. Seaver, Laurie H. Van Maldergem, Lionel Mahida, Sonal Soul, Janet S. Marlatt, Margaret Matyakhina, Ludmila Vogt, Julie Gold, June-Anne Park, Soo-Mi Varghese, Vinod Lampe, Anne K. Kumar, Ajith Lees, Melissa Holder-Espinasse, Muriel McConnell, Vivienne Bernhard, Birgitta Blair, Ed Harrison, Victoria Muzny, Donna M. Gibbs, Richard A. Elsea, Sarah H. Posey, Jennifer E. Bi, Weimin Lalani, Seema Xia, Fan Yang, Yaping Eng, Christine M. Lupski, James R. Liu, Pengfei Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_full | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_fullStr | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_full_unstemmed | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_short | Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome |
| title_sort | correction to: de novo and inherited tcf20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to smith–magenis syndrome |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6434874/ https://www.ncbi.nlm.nih.gov/pubmed/30909959 http://dx.doi.org/10.1186/s13073-019-0630-1 |
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