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                             12 results found
no title author magazine year volume issue page(s) type
1 Absence of founder BRCA1 and BRCA2 mutations in coetaneous malignant melanoma patients of Ashkenazi origin Kadouri, Luna
2008
8 1 p. 29-32
article
2 Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry Zhang, Bifeng
2008
8 1 p. 15-22
article
3 Genetic testing for BRCA1: effects of a randomised study of knowledge provision on interest in testing and long term test uptake; implications for the NICE guidelines Hall, Julia
2008
8 1 p. 5-13
article
4 Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma Mitter, Diana
2008
8 1 p. 55-58
article
5 Identification of somatic APC mutations in recurrent desmoid tumors in a patient with familial adenomatous polyposis to determine actual recurrence of the original tumor or de novo occurrence Iwama, Takeo
2008
8 1 p. 51-54
article
6 Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population Nilbert, Mef
2008
8 1 p. 75-83
article
7 MLPA mutation detection in Argentine HNPCC and FAP families Gomez, Laura C.
2008
8 1 p. 67-73
article
8 Progression to advanced neoplasia is infrequent in post colectomy familial adenomatous polyposis patients under endoscopic surveillance Gleeson, Ferga C.
2008
8 1 p. 33-38
article
9 Psychosocial impact of Peutz-Jeghers Syndrome Woo, Alice
2008
8 1 p. 59-65
article
10 The 4154delA mutation carriers in the BRCA1 gene share a common ancestry Ozolina, Silvija
2008
8 1 p. 1-4
article
11 The FAP self-concept scale (adult form) Esplen, Mary Jane
2008
8 1 p. 39-50
article
12 Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomy Gabriel, C. A.
2008
8 1 p. 23-28
article
                             12 results found
 
 Koninklijke Bibliotheek - National Library of the Netherlands