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Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene

Lynn Backers (UGent) , Bram Parton (UGent) , Marieke De Bruyne (UGent) , Simon Tavernier (UGent) , Kris Van Den Bogaert, Bart Lambrecht (UGent) , Filomeen Haerynck (UGent) and Kathleen Claes (UGent)
(2021) Research Day, Abstracts.
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Citation

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MLA
Backers, Lynn, et al. “Missing Heritability in Bloom Syndrome : First Report of a Deep-Intronic Variant Leading to Pseudo-Exon Activation in the BLM Gene.” Research Day, Abstracts, 2021.
APA
Backers, L., Parton, B., De Bruyne, M., Tavernier, S., Van Den Bogaert, K., Lambrecht, B., … Claes, K. (2021). Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene. In Research Day, Abstracts. Online meeting.
Chicago author-date
Backers, Lynn, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, and Kathleen Claes. 2021. “Missing Heritability in Bloom Syndrome : First Report of a Deep-Intronic Variant Leading to Pseudo-Exon Activation in the BLM Gene.” In Research Day, Abstracts.
Chicago author-date (all authors)
Backers, Lynn, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, and Kathleen Claes. 2021. “Missing Heritability in Bloom Syndrome : First Report of a Deep-Intronic Variant Leading to Pseudo-Exon Activation in the BLM Gene.” In Research Day, Abstracts.
Vancouver
1.
Backers L, Parton B, De Bruyne M, Tavernier S, Van Den Bogaert K, Lambrecht B, et al. Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene. In: Research Day, Abstracts. 2021.
IEEE
[1]
L. Backers et al., “Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene,” in Research Day, Abstracts, Online meeting, 2021.
@inproceedings{8693090,
  author       = {Backers, Lynn and Parton, Bram and De Bruyne, Marieke and Tavernier, Simon and Van Den Bogaert, Kris and Lambrecht, Bart and Haerynck, Filomeen and Claes, Kathleen},
  booktitle    = {Research Day, Abstracts},
  language     = {eng},
  location     = {Online meeting},
  title        = {Missing heritability in Bloom syndrome : First report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene},
  year         = {2021},
}