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Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes
| Autores principales: | , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941681/ https://www.ncbi.nlm.nih.gov/pubmed/33750428 http://dx.doi.org/10.1186/s13039-021-00534-5 |
| _version_ | 1783662176520634368 |
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| author | Coci, Emanuele G. Koehler, Udo Liehr, Thomas Stelzner, Armin Fink, Christian Langen, Hendrik Riedel, Joachim |
| author_facet | Coci, Emanuele G. Koehler, Udo Liehr, Thomas Stelzner, Armin Fink, Christian Langen, Hendrik Riedel, Joachim |
| author_sort | Coci, Emanuele G. |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-7941681 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2021 |
| publisher | BioMed Central |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-79416812021-03-09 Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes Coci, Emanuele G. Koehler, Udo Liehr, Thomas Stelzner, Armin Fink, Christian Langen, Hendrik Riedel, Joachim Mol Cytogenet Correction BioMed Central 2021-03-09 /pmc/articles/PMC7941681/ /pubmed/33750428 http://dx.doi.org/10.1186/s13039-021-00534-5 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
| spellingShingle | Correction Coci, Emanuele G. Koehler, Udo Liehr, Thomas Stelzner, Armin Fink, Christian Langen, Hendrik Riedel, Joachim Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title | Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title_full | Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title_fullStr | Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title_full_unstemmed | Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title_short | Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes |
| title_sort | correction to: canpmr syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of camta1 and nfia genes |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941681/ https://www.ncbi.nlm.nih.gov/pubmed/33750428 http://dx.doi.org/10.1186/s13039-021-00534-5 |
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