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Person
>
Entries
Stratton, MR
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created
[InstanceEdit:1614178] Rothfels, K, 2011-09-27
dbId
1614179
displayName
Stratton, MR
firstname
Michael R
initial
MR
publications
[LiteratureReference:1637891] Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes
[LiteratureReference:5661011] Natural history of Christianson syndrome
[LiteratureReference:3318337] COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer
[LiteratureReference:6799043] COSMIC: exploring the world's knowledge of somatic mutations in human cancer
[LiteratureReference:5661048] SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
[LiteratureReference:9704791] PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene
[LiteratureReference:9606466] Frequent mutation of the major cartilage collagen gene COL2A1 in chondrosarcoma
[LiteratureReference:9647073] Clinical and biological implications of driver mutations in myelodysplastic syndromes
[LiteratureReference:5672236] Mutations of the BRAF gene in human cancer
[LiteratureReference:1614272] Somatic mutations of the protein kinase gene family in human lung cancer
[LiteratureReference:2018771] Patterns of somatic mutation in human cancer genomes
schemaClass
Person
surname
Stratton
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