Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes
| Main Authors: | , , , , , , , |
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| Format: | Journal article |
| Published: |
1997
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| _version_ | 1797068527642869760 |
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| author | Tomlinson, I Beck, N Homfray, T Harocopos, C Adams, M Hodgson, S Markie, D Bodmer, W |
| author_facet | Tomlinson, I Beck, N Homfray, T Harocopos, C Adams, M Hodgson, S Markie, D Bodmer, W |
| author_sort | Tomlinson, I |
| collection | OXFORD |
| description | |
| first_indexed | 2024-03-06T22:11:53Z |
| format | Journal article |
| id | oxford-uuid:5216f06b-3bba-4b05-ba44-4f3bc3228155 |
| institution | University of Oxford |
| last_indexed | 2024-03-06T22:11:53Z |
| publishDate | 1997 |
| record_format | dspace |
| spelling | oxford-uuid:5216f06b-3bba-4b05-ba44-4f3bc32281552022-03-26T16:23:31ZMolecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5216f06b-3bba-4b05-ba44-4f3bc3228155Symplectic Elements at Oxford1997Tomlinson, IBeck, NHomfray, THarocopos, CAdams, MHodgson, SMarkie, DBodmer, W |
| spellingShingle | Tomlinson, I Beck, N Homfray, T Harocopos, C Adams, M Hodgson, S Markie, D Bodmer, W Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title | Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title_full | Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title_fullStr | Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title_full_unstemmed | Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title_short | Molecular and clinico-pathological features of two families with the HNPCC syndrome and unusual phenotypes |
| title_sort | molecular and clinico pathological features of two families with the hnpcc syndrome and unusual phenotypes |
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