1671 – 1680 of 1919
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- 2002
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Mark
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
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- Contribution to journal › Article
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Mark
Expression of NUP98/TOP1, but not of TOP1/NUP98, in a treatment-related myelodysplastic syndrome with t(10;20;11)(q24;q11;p15).
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- Contribution to journal › Article
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Mark
Unique balanced chromosome abnormalities in treatment-related myelodysplastic syndromes and acute myeloid leukemia: Report from an international workshop
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- Contribution to journal › Article
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Mark
Frequent amplification of 8q24, 11q, 17q, and 20q-specific genes in pancreatic cancer
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- Contribution to journal › Article
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Mark
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications.
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- Contribution to journal › Article
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Mark
Genomewide search for type 2 diabetes mellitus susceptibility loci in Finnish families: the Botnia study.
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- Contribution to journal › Article
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Mark
Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
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- Contribution to journal › Article
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Mark
Correlation between clinicopathological features and karyotype in 100 cartilaginous and chordoid tumours. A report from the Chromosomes and Morphology (CHAMP) Collaborative Study Group
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- Contribution to journal › Article
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Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
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- Contribution to journal › Article
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Mark
Multicolor COBRA-FISH analysis of chronic myeloid leukemia reveals novel cryptic balanced translocations during disease progression.
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- Contribution to journal › Article