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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)
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Please use this url to cite or link to this publication:

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.” RARE-MED Kick-Off Symposium, Abstracts, 2020.
APA
Backers, L., Parton, B., De Bruyne, M., Tavernier, S., Van Den Bogaert, K., Lambrecht, B., … Claes, K. (2020). Missing heritability in Bloom syndrome : first report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene. RARE-MED Kick-Off Symposium, Abstracts. Presented at the RARE-MED Kick-Off Symposium, Virtual meeting.
Chicago author-date
Backers, Lynn, Bram Parton, Marieke De Bruyne, Simon Tavernier, Kris Van Den Bogaert, Bart Lambrecht, Filomeen Haerynck, and Kathleen Claes. 2020. “Missing Heritability in Bloom Syndrome : First Report of a Deep-Intronic Variant Leading to Pseudo-Exon Activation in the BLM Gene.” In RARE-MED Kick-Off Symposium, 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. 2020. “Missing Heritability in Bloom Syndrome : First Report of a Deep-Intronic Variant Leading to Pseudo-Exon Activation in the BLM Gene.” In RARE-MED Kick-Off Symposium, 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: RARE-MED Kick-Off Symposium, Abstracts. 2020.
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 RARE-MED Kick-Off Symposium, Abstracts, Virtual meeting, 2020.
@inproceedings{8687639,
  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    = {{RARE-MED Kick-Off Symposium, Abstracts}},
  language     = {{eng}},
  location     = {{Virtual meeting}},
  title        = {{Missing heritability in Bloom syndrome : first report of a deep-intronic variant leading to pseudo-exon activation in the BLM gene}},
  year         = {{2020}},
}