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- 2006
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Mark
CHEK2*1100delC is not an important high-risk gene in families with hereditary prostate cancer in southern Sweden
(
- Contribution to journal › Article
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Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
High-risk melanoma susceptibility genes and pancreatic cancer, neural system tumors, and uveal melanoma across GenoMEL
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- Contribution to journal › Article
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Mark
High-resolution genome-wide array-based comparative genome hybridization reveals cryptic chromosome changes in AML and MDS cases with trisomy 8 as the sole cytogenetic aberration.
(
- Contribution to journal › Article
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Mark
p53 mutation and cyclin D1 amplification correlate with cisplatin sensitivity in xenografted human squamous cell carcinomas from head and neck.
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- Contribution to journal › Article
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Mark
Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies
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- Contribution to journal › Article
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Mark
Protein Expression Profiling of Hereditary Breast Cancer
2006) 7th Siena Meeting, From Genome to Proteome: Biomarker Discovery & Imaging Proteomes(
- Contribution to conference › Abstract
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Mark
Protein Expression Profiling of Hereditary Breast Cancer
2006) 5th annual HUPO world congress, 2006(
- Contribution to conference › Abstract
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Mark
Chromosome 5 imbalance mapping in breast tumors from BRCA1 and BRCA2 mutation carriers and sporadic breast tumors
(
- Contribution to journal › Article
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Mark
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
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- Contribution to journal › Letter