Identification of a mutation in exon 27 of the RB1 gene associated with incomplete penetrance retinoblastoma.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 55, doi. 10.1007/s10689-008-9198-4
- By:
- Publication type:
- Article
Works matching IS 13899600 AND DT 2009 AND VI 8 AND IP 1
Results: 12
1
2
Progression to advanced neoplasia is infrequent in post colectomy familial adenomatous polyposis patients under endoscopic surveillance.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 33, doi. 10.1007/s10689-008-9203-y
- By:
- Publication type:
- Article
3
Evidence for an ancient BRCA1 mutation in breast cancer patients of yoruban ancestry.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 15, doi. 10.1007/s10689-008-9205-9
- By:
- Publication type:
- Article
4
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.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 51, doi. 10.1007/s10689-008-9207-7
- By:
- Publication type:
- Article
5
Major contribution from recurrent alterations and MSH6 mutations in the Danish Lynch syndrome population.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 75, doi. 10.1007/s10689-008-9199-3
- By:
- Publication type:
- Article
6
Psychosocial impact of Peutz-Jeghers Syndrome.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 59, doi. 10.1007/s10689-008-9202-z
- By:
- Publication type:
- Article
7
MLPA mutation detection in Argentine HNPCC and FAP families.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 67, doi. 10.1007/s10689-008-9200-1
- By:
- Publication type:
- Article
8
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.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 5, doi. 10.1007/s10689-008-9201-0
- By:
- Publication type:
- Article
9
Absence of founder BRCA1 and BRCA2 mutations in coetaneous malignant melanoma patients of Ashkenazi origin.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 29, doi. 10.1007/s10689-008-9206-8
- By:
- Publication type:
- Article
10
The FAP self-concept scale (adult form).
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 39, doi. 10.1007/s10689-008-9204-x
- By:
- Publication type:
- Article
11
Use of total abdominal hysterectomy and hormone replacement therapy in BRCA1 and BRCA2 mutation carriers undergoing risk-reducing salpingo-oophorectomy.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 23, doi. 10.1007/s10689-008-9208-6
- By:
- Publication type:
- Article
12
The 4154delA mutation carriers in the BRCA1 gene share a common ancestry.
- Published in:
- Familial Cancer, 2009, v. 8, n. 1, p. 1, doi. 10.1007/s10689-008-9224-6
- By:
- Publication type:
- Article