Revision history of "COMPREHENSIVE ANALYSIS OF GENETIC FACTORS PREDISPOSING TO GENOMIC DISORDERS. DIGEORGE/VELOCARDIOFACIAL SYNDROME AS A STUDY MODEL" (Q3171576)

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23 March 2024

20 December 2023

12 June 2023

10 June 2023

18 August 2022

  • curprev 03:0703:07, 18 August 2022DG Regio talk contribs 84,624 bytes +58,480 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 18:1918:19, 12 October 2021DG Regio talk contribs 13,638 bytes +2,826 Created claim: summary (P836): RESEARCH ON GENOMIC DISORDERS AND RARE DISEASES HAS MAINLY FOCUSED ON CLINICAL DIAGNOSIS. HOWEVER, KNOWLEDGE OF THE MOLECULAR CAUSES GENERATED BY THESE ANOMALIES IS ALSO A FUNDAMENTAL ASPECT FOR DETERMINING THE UNDERLYING CAUSES OF THESE GENETIC PATHOLOGIES. The PROJECT PRESENTATE COMBIN INVESTIGATION BASIC AND INVESTIGATION APPLICED TO CLINICAL AND IS OF CHARACTER NEWS WITH RESPECT TO EXPERIMENTAL TECHNICAL AND Methodologies AND THE PUBLICATIO...
  • curprev 18:1918:19, 12 October 2021DG Regio talk contribs 10,812 bytes −2,826 Removed claim: summary (P836): RESEARCH ON GENOMIC DISORDERS AND RARE DISEASES HAS MAINLY FOCUSED ON CLINICAL DIAGNOSIS. HOWEVER, KNOWLEDGE OF THE MOLECULAR CAUSES GENERATED BY THESE ANOMALIES IS ALSO A FUNDAMENTAL ASPECT FOR DETERMINING THE UNDERLYING CAUSES OF THESE GENETIC PATHOLOGIES. The PROJECT PRESENTATE COMBIN INVESTIGATION BASIC AND INVESTIGATION APPLICED TO CLINICAL AND IS OF CHARACTER NEWS WITH RESPECT TO EXPERIMENTAL TECHNICAL AND Methodologies AND THE PUBLICAT...
  • curprev 18:0018:00, 12 October 2021DG Regio talk contribs 13,638 bytes +188 Changed label, description and/or aliases in en: translated_label
  • curprev 18:0018:00, 12 October 2021DG Regio talk contribs 13,450 bytes +2,826 Created claim: summary (P836): RESEARCH ON GENOMIC DISORDERS AND RARE DISEASES HAS MAINLY FOCUSED ON CLINICAL DIAGNOSIS. HOWEVER, KNOWLEDGE OF THE MOLECULAR CAUSES GENERATED BY THESE ANOMALIES IS ALSO A FUNDAMENTAL ASPECT FOR DETERMINING THE UNDERLYING CAUSES OF THESE GENETIC PATHOLOGIES. The PROJECT PRESENTATE COMBIN INVESTIGATION BASIC AND INVESTIGATION APPLICED TO CLINICAL AND IS OF CHARACTER NEWS WITH RESPECT TO EXPERIMENTAL TECHNICAL AND Methodologies AND THE PUBLICATIO...

10 October 2021

9 October 2021

8 October 2021