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1 t some clinical overlap, Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.
2 sia syndromes, including Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome.
3 EN have been shown to cause Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome and Proteus syndrome.
4 or syndrome (including Cowden's syndrome and Bannayan-Riley-Ruvalcaba syndrome), and hereditary mixed
5                     Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome are allelic, defined b
6 TEN mutations cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), two hamartoma-t
7 TEN mutations cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), two hamartoma-t
8 e clinical overlap, Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR).
9 r hamartomatous polyposis syndromes, such as Bannayan-Riley-Ruvalcaba syndrome (BRRS) and Cowden dise
10 other inherited hamartoma syndromes, such as Bannayan-Riley-Ruvalcaba syndrome (BRRS) and Cowden synd
11                     Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS) are autosomal d
12                                              Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare hamar
13 sk of breast and thyroid cancers, and 65% of Bannayan-Riley-Ruvalcaba syndrome (BRRS), characterized
14 of individuals with Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS), respectively.
15 owden syndrome (CS) and 60% of patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).
16 mes, including both Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS).
17 ase on 10q23, cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS).
18 ns cause subsets of Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS); these subsets
19                                              Bannayan-Riley-Ruvalcaba syndrome is a congenital syndro
20 The three hamartomatous polyposis syndromes, Bannayan-Riley-Ruvalcaba syndrome, juvenile polyposis co
21                   It has been suggested that Bannayan-Riley-Ruvalcaba syndrome may be a variant of ju
22 how that cell lines from Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients with germ lin
23 rlapping clinical features: Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome and
24 yndrome" (PHTS) and include Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome, and
25 reast, thyroid, and endometrial cancers, and Bannayan-Riley-Ruvalcaba syndrome, which is characterize