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Page 1
The natural history of autosomal dominant polycystic kidney disease. A strategy for grouping families and mutations.
Nefrologia (Engl Ed). 2023 Jan-Feb;43(1):120-125. doi: 10.1016/j.nefroe.2023.03.010. Epub 2023 May 31.
Nefrologia (Engl Ed). 2023.
PMID: 37268502
Free article.
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. Among authors: espejo portero i.
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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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: espejo portero i.
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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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: espejo portero i.
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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[Partial trisomy and mosaicism associated with Fallot Tetralogy].
Tejero Hernández MA, Gómez Guzmán E, Espejo Portero I, Barcos M.
Tejero Hernández MA, et al. Among authors: espejo portero i.
An Pediatr (Barc). 2011 Jan;74(1):55-6. doi: 10.1016/j.anpedi.2010.08.004. Epub 2010 Dec 10.
An Pediatr (Barc). 2011.
PMID: 20971045
Free article.
Spanish.
No abstract available.
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