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Page 1
Language Impairment Resulting from a de novo Deletion of 7q32.1q33.
Mol Syndromol. 2016 Oct;7(5):292-298. doi: 10.1159/000448208. Epub 2016 Aug 6.
Mol Syndromol. 2016.
PMID: 27867345
Free PMC article.
Variable Penetrance of the 15q11.2 BP1-BP2 Microduplication in a Family with Cognitive and Language Impairment.
Benítez-Burraco A, Barcos-Martínez M, Espejo-Portero I, Jiménez-Romero S.
Benítez-Burraco A, et al. Among authors: barcos martinez m.
Mol Syndromol. 2017 May;8(3):139-147. doi: 10.1159/000468192. Epub 2017 Apr 14.
Mol Syndromol. 2017.
PMID: 28588435
Free PMC article.
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Spanish multidisciplinary clinical practice guidelines for Anderson-Fabry Disease in Adults. I. Method and recommendations.
Calderón Sandubete EJ, Briones Pérez de la Blanca E, Alonso-Ortiz Del Río C, Santamaría Olmo R, López Mendoza M, Barcos Martínez M, Márquez Infante C, Marín-León I; en nombre del Grupo Guía Fabry.
Calderón Sandubete EJ, et al. Among authors: barcos martinez m.
Rev Clin Esp (Barc). 2019 May;219(4):200-207. doi: 10.1016/j.rce.2018.09.017. Epub 2019 Jan 26.
Rev Clin Esp (Barc). 2019.
PMID: 30691688
English, Spanish.
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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: barcos martinez 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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