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- 2019
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Mark
Functional characterization of novel germline TP53 variants in Swedish families
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- Contribution to journal › Article
- 2018
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Mark
Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication
(
- Contribution to journal › Article
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Mark
Enrichment of rare copy number variation in children with developmental language disorder
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- Contribution to journal › Article
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Mark
How do consent forms for diagnostic high-throughput sequencing address unsolicited and secondary findings? A content analysis
(
- Contribution to journal › Article
- 2017
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Mark
Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation
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- Contribution to journal › Article