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...
Những tác giả chính: | 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 |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
2014
|
Những quyển sách tương tự
-
InSiGHT leads in the implementation of the Human Variome Project
Bằng: Macrae Finlay, et al.
Được phát hành: (2011-03-01) -
the niGHt EtERnAL /
Bằng: Toro, Guillermo del, 1964-, author, et al.
Được phát hành: (2011) -
Disease-causing gene-flanking genomic rearrangements in HNPCC patients
Bằng: Morak Monika, et al.
Được phát hành: (2011-03-01) -
Design Procedure of a Mono-Anchor Head for 2360 MPa High-Strength Steel Strand
Bằng: Sang-Woo Ko, et al.
Được phát hành: (2023-02-01) -
2360 Engaging, capturing, and integrating the voice of the customer and collaborator in a clinical and translational science program
Bằng: Boris Volkov, et al.
Được phát hành: (2018-06-01)