Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome
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| Veröffentlicht in: | Frontiers in pediatrics 2018, Vol.6, p.163-163 |
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| Sprache: | eng |
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| container_start_page | 163 |
| container_title | Frontiers in pediatrics |
| container_volume | 6 |
| creator | Benítez-Burraco, Antonio Barcos-Martínez, Montserrat Espejo-Portero, Isabel Fernández-Urquiza, Maite Torres-Ruiz, Raúl Rodríguez-Perales, Sandra Jiménez-Romero, Ma Salud |
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| doi_str_mv | 10.3389/fped.2018.00163 |
| format | Report |
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| fulltext | fulltext |
| identifier | ISSN: 2296-2360 |
| ispartof | Frontiers in pediatrics, 2018, Vol.6, p.163-163 |
| issn | 2296-2360 2296-2360 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_2057437673 |
| source | DOAJ Directory of Open Access Journals; PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central |
| title | Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome |
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