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- 2006
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Mark
Complement deficiency and disease: An update.
(
- Contribution to journal › Scientific review
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Mark
Influence of methotrexate, TNF blockers and prednisolone on antibody responses to pneumococcal polysaccharide vaccine in patients with rheumatoid arthritis.
(
- Contribution to journal › Article
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Mark
Homozygosity for the IgG2 subclass allotype G2M(n) protects against severe infection in hereditary C2 deficiency
(
- 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
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- 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
(
- Contribution to journal › Letter
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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
- 2005
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Mark
Genetic characterization of malignant melanoma and breast cancer
(
- Thesis › Doctoral thesis (compilation)
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Mark
Hereditary C2 Deficiency in Sweden: Frequent Occurrence of Invasive Infection, Atherosclerosis, and Rheumatic Disease.
(
- Contribution to journal › Article
-
Mark
Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith-Magenis syndrome minimum deletion to similar to 650 kb
(
- Contribution to journal › Article