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Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598310/ https://www.ncbi.nlm.nih.gov/pubmed/22909776 http://dx.doi.org/10.1038/ejhg.2012.166 |
| _version_ | 1782262749206675456 |
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| author | Newbury, Dianne F Mari, Francesca Sadighi Akha, Elham MacDermot, Kay D Canitano, Roberto Monaco, Anthony P Taylor, Jenny C Renieri, Alessandra Fisher, Simon E Knight, Samantha J L |
| author_facet | Newbury, Dianne F Mari, Francesca Sadighi Akha, Elham MacDermot, Kay D Canitano, Roberto Monaco, Anthony P Taylor, Jenny C Renieri, Alessandra Fisher, Simon E Knight, Samantha J L |
| author_sort | Newbury, Dianne F |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-3598310 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2013 |
| publisher | Nature Publishing Group |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-35983102013-04-01 Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder Newbury, Dianne F Mari, Francesca Sadighi Akha, Elham MacDermot, Kay D Canitano, Roberto Monaco, Anthony P Taylor, Jenny C Renieri, Alessandra Fisher, Simon E Knight, Samantha J L Eur J Hum Genet Letter Nature Publishing Group 2013-04 2012-08-22 /pmc/articles/PMC3598310/ /pubmed/22909776 http://dx.doi.org/10.1038/ejhg.2012.166 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/ |
| spellingShingle | Letter Newbury, Dianne F Mari, Francesca Sadighi Akha, Elham MacDermot, Kay D Canitano, Roberto Monaco, Anthony P Taylor, Jenny C Renieri, Alessandra Fisher, Simon E Knight, Samantha J L Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title_full | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title_fullStr | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title_full_unstemmed | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title_short | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| title_sort | dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder |
| topic | Letter |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3598310/ https://www.ncbi.nlm.nih.gov/pubmed/22909776 http://dx.doi.org/10.1038/ejhg.2012.166 |
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