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- Conference Paper
- C3
- open access
Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation
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Long-read sequencing and optical genome mapping enable full characterization of previously unresolved structural variation
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- Journal Article
- A2
- open access
Pushing the boundaries : concurrent Hodgkin lymphoma and breast cancer treatment with preservation of pregnancy : a case report
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Prenatally detected copy number variants in a national cohort : a postnatal follow-up study
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The Belgian MicroArray Prenatal (BEMAPRE) database : a systematic nationwide repository of fetal genomic aberrations
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Genome-wide copy number variation scan identifies complement component C4 as novel susceptibility gene for Crohn's disease
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- Journal Article
- A1
- open access
arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays