Division of Clinical Genetics
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- 2008
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Mark
Delection of the SCN gene cluster on 2q24.4 is associated with severe epilepsy an array-based genotype-phenotype correlation and a comprehensive review of previously published area
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- Contribution to journal › Article
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Mark
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
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- Contribution to journal › Article
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Mark
Recurrent and multiple bladder tumors show conserved expression profiles.
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- Contribution to journal › Article
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Mark
Binomial mitotic segregation of MYCN-carrying double minutes in neuroblastoma illustrates the role of randomness in oncogene amplification.
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- Contribution to journal › Article
- 2007
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Mark
The impact of translocations and gene fusions on cancer causation.
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- Contribution to journal › Scientific review
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Mark
Concurrent gain of 17q and the MYC oncogene in a medullomyoblastoma
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- Contribution to journal › Article
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Mark
Tiling resolution array comparative genomic hybridization, expression and methylation analyses of dup(1q) in Burkitt lymphomas and pediatric high hyperdiploid acute lymphoblastic leukemias reveal clustered near-centromeric breakpoints and overexpression of genes in 1q22-32.3
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- Contribution to journal › Article
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Mark
A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families
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- Contribution to journal › Article
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Mark
Threshold-free high-power methods for the ontological analysis of genome-wide gene expression studies
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- Contribution to journal › Article
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Mark
Generation of human cortical neurons from a new immortal fetal neural stem cell line.
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- Contribution to journal › Article