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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2017 | 1 |
2018 | 2 |
2020 | 2 |
2021 | 1 |
2022 | 3 |
2023 | 1 |
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Page 1
Language impairment with a microduplication in 1q42.3q43.
Clin Linguist Phon. 2021 Jul 3;35(7):610-635. doi: 10.1080/02699206.2020.1812119. Epub 2020 Aug 28.
Clin Linguist Phon. 2021.
PMID: 32856472
Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome.
Jiménez-Romero MS, Fernández-Urquiza M, Benítez-Burraco A.
Jiménez-Romero MS, et al. Among authors: fernandez urquiza m.
J Speech Lang Hear Res. 2022 Dec 12;65(12):4724-4740. doi: 10.1044/2022_JSLHR-22-00160. Epub 2022 Nov 21.
J Speech Lang Hear Res. 2022.
PMID: 36410413
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Language Impairment with a Partial Duplication of DOCK8.
Benítez-Burraco A, Fernández-Urquiza M, Jiménez-Romero MS.
Benítez-Burraco A, et al. Among authors: fernandez urquiza m.
Mol Syndromol. 2020 Dec;11(5-6):243-263. doi: 10.1159/000511972. Epub 2020 Dec 11.
Mol Syndromol. 2020.
PMID: 33510598
Free PMC article.
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Pragmatic Profiles of Adults with Fragile X Syndrome and Williams Syndrome.
Diez-Itza E, Viejo A, Fernández-Urquiza M.
Diez-Itza E, et al. Among authors: fernandez urquiza m.
Brain Sci. 2022 Mar 13;12(3):385. doi: 10.3390/brainsci12030385.
Brain Sci. 2022.
PMID: 35326341
Free PMC article.
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Explicit Oral Narrative Intervention for Students with Williams Syndrome.
Diez-Itza E, Martínez V, Pérez V, Fernández-Urquiza M.
Diez-Itza E, et al. Among authors: fernandez urquiza m.
Front Psychol. 2018 Jan 15;8:2337. doi: 10.3389/fpsyg.2017.02337. eCollection 2017.
Front Psychol. 2018.
PMID: 29379455
Free PMC article.
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Delving into the Genetic Causes of Language Impairment in a Case of Partial Deletion of NRXN1.
Benítez-Burraco A, Jiménez-Romero MS, Fernández-Urquiza M.
Benítez-Burraco A, et al. Among authors: fernandez urquiza m.
Mol Syndromol. 2023 Jan;13(6):496-510. doi: 10.1159/000524710. Epub 2022 Jun 14.
Mol Syndromol. 2023.
PMID: 36660026
Free PMC article.
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Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.
Benítez-Burraco A, Barcos-Martínez M, Espejo-Portero I, Fernández-Urquiza M, Torres-Ruiz R, Rodríguez-Perales S, Jiménez-Romero MS.
Benítez-Burraco A, et al. Among authors: fernandez urquiza m.
Front Pediatr. 2018 Jun 5;6:163. doi: 10.3389/fped.2018.00163. eCollection 2018.
Front Pediatr. 2018.
PMID: 29922639
Free PMC article.
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