Revision history of "Creation of a tool (NeuroMeGen) for the diagnosis of congenital neurometabolic diseases and implementation in the SNS" (Q3161294)

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22 March 2024

20 December 2023

12 June 2023

10 June 2023

18 August 2022

  • curprev 00:5000:50, 18 August 2022DG Regio talk contribs 76,305 bytes +52,612 Changed label, description and/or aliases in el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl, nl, fr, de, it, es, and other parts: Adding translations: el, da, fi, mt, lv, sk, ga, cs, pt, et, hu, bg, lt, hr, sv, ro, sl, pl,

16 January 2022

17 December 2021

9 December 2021

4 December 2021

12 October 2021

  • curprev 17:0717:07, 12 October 2021DG Regio talk contribs 12,789 bytes +177 Changed label, description and/or aliases in en: translated_label
  • curprev 17:0717:07, 12 October 2021DG Regio talk contribs 12,612 bytes +2,343 Created claim: summary (P836): One of the most difficult challenges facing specialists is the diagnosis of patients with phenotypic signs and symptoms that suggest an underlying genetic cause, but for whom etiology remains elusive despite costly and often lengthy etiological research. The purpose of this project is to create a diagnostic tool based on mass sequencing technology, phenotypic analysis and pattern recognition that facilitates the diagnosis of neurometabolic disor...

10 October 2021

9 October 2021

8 October 2021