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Year | Number of Results |
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1980 | 1 |
2001 | 1 |
2008 | 1 |
2017 | 1 |
2019 | 1 |
2021 | 1 |
2024 | 0 |
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Page 1
The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.
Sci Rep. 2017 Sep 25;7(1):12288. doi: 10.1038/s41598-017-11620-3.
Sci Rep. 2017.
PMID: 28947817
Free PMC article.
Author Correction: The utility of Next Generation Sequencing for molecular diagnostics in Rett syndrome.
Vidal S, Brandi N, Pacheco P, Gerotina E, Blasco L, Trotta JR, Derdak S, Del Mar O'Callaghan M, Garcia-Cazorla À, Pineda M, Armstrong J; Rett Working Group.
Vidal S, et al.
Sci Rep. 2021 Sep 7;11(1):18146. doi: 10.1038/s41598-021-97262-y.
Sci Rep. 2021.
PMID: 34493777
Free PMC article.
No abstract available.
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X chromosome inactivation does not necessarily determine the severity of the phenotype in Rett syndrome patients.
Xiol C, Vidal S, Pascual-Alonso A, Blasco L, Brandi N, Pacheco P, Gerotina E, O'Callaghan M, Pineda M, Armstrong J; Rett Working Group.
Xiol C, et al.
Sci Rep. 2019 Aug 19;9(1):11983. doi: 10.1038/s41598-019-48385-w.
Sci Rep. 2019.
PMID: 31427717
Free PMC article.
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Rett syndrome in Spain: mutation analysis and clinical correlations.
Monrós E, Armstrong J, Aibar E, Poo P, Canós I, Pineda M.
Monrós E, et al. Among authors: canos i.
Brain Dev. 2001 Dec;23 Suppl 1:S251-3. doi: 10.1016/s0387-7604(01)00374-6.
Brain Dev. 2001.
PMID: 11738885
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Clinical laboratory automated urinalysis: comparison among automated microscopy, flow cytometry, two test strips analyzers, and manual microscopic examination of the urine sediments.
Mayo S, Acevedo D, Quiñones-Torrelo C, Canós I, Sancho M.
Mayo S, et al. Among authors: canos i.
J Clin Lab Anal. 2008;22(4):262-70. doi: 10.1002/jcla.20257.
J Clin Lab Anal. 2008.
PMID: 18623125
Free PMC article.
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[A rare case of silent cholinesterase genetic variant (author's transl)].
Otte A, Bonilla I, Gil C, Bolinches R, Andreu L, Canós I.
Otte A, et al. Among authors: canos i.
Med Clin (Barc). 1980 Oct 25;75(7):309-11.
Med Clin (Barc). 1980.
PMID: 7432039
Spanish.
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