Revision history of "HEMOLYTIC ANEMIA. MOLECULAR DIAGNOSIS BY MASS SEQUENCING (NGS)" (Q3162019)

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7 March 2024

20 December 2023

12 June 2023

10 June 2023

4 August 2022

  • curprev 09:2309:23, 4 August 2022DG Regio talk contribs 70,748 bytes +48,142 Changed label, description and/or aliases in et, lt, hr, el, sk, fi, pl, hu, cs, lv, ga, sl, bg, mt, pt, da, ro, sv, nl, fr, de, it, es, and other parts: Adding translations: et, lt, hr, el, sk, fi, pl, hu, cs, lv, ga, sl, bg, mt, pt, da, ro, sv,

16 January 2022

17 December 2021

9 December 2021

4 December 2021

12 October 2021

  • curprev 18:3918:39, 12 October 2021DG Regio talk contribs 12,357 bytes +2,254 Created claim: summary (P836): The objective of this project is to corroborate the design and development of a panel of genes of mass sequencing (Next Generation Sequencing), for the molecular genetic diagnosis of patients with congenital hemolytic anemia, in any of its varieties. An extensive bibliographic review of the variants detected in the genes involved in hemolytic anemias has been carried out and based on this review 25 genes have been selected for variants that dire...
  • curprev 18:3918:39, 12 October 2021DG Regio talk contribs 10,103 bytes −2,254 Removed claim: summary (P836): The objective of this project is to corroborate the design and development of a panel of genes of mass sequencing (Next Generation Sequencing), for the molecular genetic diagnosis of patients with congenital hemolytic anemia, in any of its varieties. An extensive bibliographic review of the variants detected in the genes involved in hemolytic anemias has been carried out and based on this review 25 genes have been selected for variants that di...
  • curprev 18:0818:08, 12 October 2021DG Regio talk contribs 12,357 bytes +121 Changed label, description and/or aliases in en: translated_label
  • curprev 18:0818:08, 12 October 2021DG Regio talk contribs 12,236 bytes +2,254 Created claim: summary (P836): The objective of this project is to corroborate the design and development of a panel of genes of mass sequencing (Next Generation Sequencing), for the molecular genetic diagnosis of patients with congenital hemolytic anemia, in any of its varieties. An extensive bibliographic review of the variants detected in the genes involved in hemolytic anemias has been carried out and based on this review 25 genes have been selected for variants that dire...

10 October 2021

9 October 2021

8 October 2021