Literature DB >> 31647332

Correct application of variant classification guidelines in germline RUNX1 mutated disorders to assist clinical diagnosis.

Anna L Brown1,2,3, Christopher Hahn1,2,3, Devendra Hiwase3,4,5, Lucy A Godley6,7, Hamish S Scott1,2,3.   

Abstract

Entities:  

Year:  2019        PMID: 31647332     DOI: 10.1080/10428194.2019.1680842

Source DB:  PubMed          Journal:  Leuk Lymphoma        ISSN: 1026-8022


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  1 in total

1.  The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy.

Authors:  Claire C Homan; Sarah L King-Smith; David M Lawrence; Peer Arts; Jinghua Feng; James Andrews; Mark Armstrong; Thuong Ha; Julia Dobbins; Michael W Drazer; Kai Yu; Csaba Bödör; Alan Cantor; Mario Cazzola; Erin Degelman; Courtney D DiNardo; Nicolas Duployez; Remi Favier; Stefan Fröhling; Jude Fitzgibbon; Jeffery M Klco; Alwin Krämer; Mineo Kurokawa; Joanne Lee; Luca Malcovati; Neil V Morgan; Georges Natsoulis; Carolyn Owen; Keyur P Patel; Claude Preudhomme; Hana Raslova; Hugh Rienhoff; Tim Ripperger; Rachael Schulte; Kiran Tawana; Elvira Velloso; Benedict Yan; Paul Liu; Lucy A Godley; Andreas W Schreiber; Christopher N Hahn; Hamish S Scott; Anna L Brown
Journal:  Haematologica       Date:  2021-11-01       Impact factor: 9.941

  1 in total

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