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- 2001
-
Mark
Genetic epidemiology of BRCA1 mutations in Norway
(
- Contribution to journal › Article
-
Mark
First BRCA1 and BRCA2 gene testing implemented in the health care system of Stockholm
(
- Contribution to journal › Article
-
Mark
Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families
(
- Contribution to journal › Article
- 2000
-
Mark
MYB oncogene amplification in hereditary BRCA1 breast cancer
(
- Contribution to journal › Article
-
Mark
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation
(
- Contribution to journal › Article
-
Mark
Somatic frameshift alterations in mononucleotide repeat-containing genes in different tumor types from an HNPCC family with germline MSH2 mutation
(
- Contribution to journal › Article
-
Mark
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
(
- Contribution to journal › Article
-
Mark
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
(
- Contribution to journal › Article
-
Mark
BRCA1 and BRCA2 mutations in ovarian cancer : Covariation with specific cytogenetic features
(
- Contribution to journal › Article
-
Mark
Prognosis and clinical presentation of BRCA2-associated breast cancer
(
- Contribution to journal › Article