Åke Borg
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- 2006
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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
- Contribution to journal › Letter
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Mark
Gene expression profiles relate to SS18/SSX fusion type in synovial sarcoma
- Contribution to journal › Article
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Mark
Characterisation of dic(9;20)(p11-13;q11) in childhood B-cell precursor acute lymphoblastic leukaemia by tiling resolution array-based comparative genomic hybridisation reveals clustered breakpoints at 9p13.2 and 20q11.2
- Contribution to journal › Article
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Mark
RAD50 and NBS1 are breast cancer susceptibility genes associated with genomic instability
- 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.
- Contribution to journal › Article
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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
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
- Contribution to journal › Letter
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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.
- 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
- Contribution to journal › Article
