Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
The clinical classification of hereditary sequence variants identified in disease-related genes directly affects clinical management of patients and their relatives. The International Society for Gastrointestinal Hereditary Tumours (InSiGHT) undertook a collaborative effort to develop, test and appl...
Հիմնական հեղինակներ: | Thompson, B, Spurdle, AB, Plazzer, J, Greenblatt, MS, Akagi, K, Al-Mulla, F, Bapat, B, Bernstein, I, Capellá, G, den Dunnen, J, du Sart, D, Fabre, A, Farrell, M, Farrington, S, Frayling, I, Frebourg, T, Goldgar, D, Heinen, C, Holinski-Feder, E, Kohonen-Corish, M, Robinson, K, Leung, S, Martins, A, Moller, P, Morak, M |
---|---|
Ձևաչափ: | Journal article |
Լեզու: | English |
Հրապարակվել է: |
2014
|
Նմանատիպ նյութեր
-
InSiGHT leads in the implementation of the Human Variome Project
: Macrae Finlay, և այլն
Հրապարակվել է: (2011-03-01) -
the niGHt EtERnAL /
: Toro, Guillermo del, 1964-, author, և այլն
Հրապարակվել է: (2011) -
Disease-causing gene-flanking genomic rearrangements in HNPCC patients
: Morak Monika, և այլն
Հրապարակվել է: (2011-03-01) -
Design Procedure of a Mono-Anchor Head for 2360 MPa High-Strength Steel Strand
: Sang-Woo Ko, և այլն
Հրապարակվել է: (2023-02-01) -
2360 Engaging, capturing, and integrating the voice of the customer and collaborator in a clinical and translational science program
: Boris Volkov, և այլն
Հրապարակվել է: (2018-06-01)