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Novel Electromagnetic Characterization Methods for New Materials and Structures in Aerospace Platforms.
Materials (Basel). 2022 Jul 23;15(15):5128. doi: 10.3390/ma15155128.
Materials (Basel). 2022.
PMID: 35897561
Free PMC article.
Characterization of Joints between Carbon Fiber Composite Parts Using a Microstrip Transmission Line Method.
Plaza B, López D, Poyatos D.
Plaza B, et al. Among authors: poyatos d.
Sensors (Basel). 2021 Feb 6;21(4):1142. doi: 10.3390/s21041142.
Sensors (Basel). 2021.
PMID: 33562004
Free PMC article.
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[Prader Willi syndrome patients: study of 77 patients].
Poyatos D, Camprubí C, Gabau E, Nosas R, Villatoro S, Coll MD, Guitart M.
Poyatos D, et al.
Med Clin (Barc). 2009 Nov 7;133(17):649-56. doi: 10.1016/j.medcli.2009.04.051. Epub 2009 Sep 13.
Med Clin (Barc). 2009.
PMID: 19748638
Spanish.
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Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
Camprubí C, Coll MD, Villatoro S, Gabau E, Kamli A, Martínez MJ, Poyatos D, Guitart M.
Camprubí C, et al. Among authors: poyatos d.
Eur J Med Genet. 2007 Jan-Feb;50(1):11-20. doi: 10.1016/j.ejmg.2006.10.001. Epub 2006 Oct 10.
Eur J Med Genet. 2007.
PMID: 17095305
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Severe phenotype in Angelman syndrome resulting from paternal isochromosome 15.
Poyatos D, Guitart M, Gabau E, Brun C, Mila M, Vaquerizo J, Coll MD.
Poyatos D, et al.
J Med Genet. 2002 Feb;39(2):E4. doi: 10.1136/jmg.39.2.e4.
J Med Genet. 2002.
PMID: 11836373
Free PMC article.
No abstract available.
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Confirmation of Angelman syndrome in a boy previously reported as having Becker muscular dystrophy and severe mental retardation.
Poyatos D, Coll MD, Guitart M, Colomer J.
Poyatos D, et al.
Eur J Pediatr. 1999 Dec;158(12):1006. doi: 10.1007/s004310051269.
Eur J Pediatr. 1999.
PMID: 10592081
No abstract available.
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