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- 2000
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Mark
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
(
- Contribution to journal › Article
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Mark
Prognosis and clinical presentation of BRCA2-associated breast cancer
(
- Contribution to journal › Article
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Mark
BRCA1 and BRCA2 mutations in ovarian cancer : Covariation with specific cytogenetic features
(
- Contribution to journal › Article
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Mark
A hypersensitive estrogen receptor-alpha mutation in premalignant breast lesions
(
- Contribution to journal › Article
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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
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Mark
High frequency of multiple melanomas and breast and pancreas carcinomas in CDKN2A mutation-positive melanoma families
(
- Contribution to journal › Article
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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
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Mark
MYB oncogene amplification in hereditary BRCA1 breast cancer
(
- Contribution to journal › Article
- 1999
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Mark
Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations
(
- Contribution to journal › Article
-
Mark
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
(
- Contribution to journal › Article