ライフサイエンスコーパス: Bannayan-Riley-Ruvalcaba syndrome

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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 Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome are allelic, defined b

5 TEN mutations cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), two hamartoma-t

6 TEN mutations cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), two hamartoma-t

7 e clinical overlap, Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR).

8 r hamartomatous polyposis syndromes, such as Bannayan-Riley-Ruvalcaba syndrome (BRRS) and Cowden dise

9 other inherited hamartoma syndromes, such as Bannayan-Riley-Ruvalcaba syndrome (BRRS) and Cowden synd

10 Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS) are autosomal d

11 Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare hamar

12 sk of breast and thyroid cancers, and 65% of Bannayan-Riley-Ruvalcaba syndrome (BRRS), characterized

13 of individuals with Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS), respectively.

14 mes, including both Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS).

15 owden syndrome (CS) and 60% of patients with Bannayan-Riley-Ruvalcaba syndrome (BRRS).

16 ase on 10q23, cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRRS).

17 Bannayan-Riley-Ruvalcaba syndrome is a congenital syndro

18 The three hamartomatous polyposis syndromes, Bannayan-Riley-Ruvalcaba syndrome, juvenile polyposis co

19 It has been suggested that Bannayan-Riley-Ruvalcaba syndrome may be a variant of ju

20 how that cell lines from Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients with germ lin

21 rlapping clinical features: Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome and

22 yndrome" (PHTS) and include Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus syndrome, and

23 reast, thyroid, and endometrial cancers, and Bannayan-Riley-Ruvalcaba syndrome, which is characterize

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