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Page 1
Language and Communication Deficits in Chromosome 16p11.2 Deletion Syndrome.
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
Language Impairment with a Partial Duplication of DOCK8.
Benítez-Burraco A, Fernández-Urquiza M, Jiménez-Romero MS.
Benítez-Burraco A, et al. Among authors: jimenez romero ms.
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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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: jimenez romero ms.
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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Language Impairment Resulting from a de novo Deletion of 7q32.1q33.
Jiménez-Romero MS, Barcos-Martínez M, Espejo-Portero I, Benítez-Burraco A.
Jiménez-Romero MS, et al.
Mol Syndromol. 2016 Oct;7(5):292-298. doi: 10.1159/000448208. Epub 2016 Aug 6.
Mol Syndromol. 2016.
PMID: 27867345
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: jimenez romero ms.
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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The influence of cochlear implants on behaviour problems in deaf children.
Jiménez-Romero MS.
Jiménez-Romero MS.
Psicothema. 2015;27(3):229-34. doi: 10.7334/psicothema2014.269.
Psicothema. 2015.
PMID: 26260929
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