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Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing

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Citation

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

MLA
Ascari, Giulia, et al. “Unraveling Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss Using Long-Read Sequencing.” Genetics of Ocular Development (GoOD) Meeting, Abstracts, 2020.
APA
Ascari, G., Rendtorff, N. D., Jacob, J., De Zaeytijd, J., Baumont, V., De Bruyne, M., … De Baere, E. (2020). Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing. Genetics of Ocular Development (GoOD) Meeting, Abstracts. Presented at the Genetics of Ocular Development (GoOD) meeting, Paris, France.
Chicago author-date
Ascari, Giulia, Nanna D. Rendtorff, Julie Jacob, Julie De Zaeytijd, Valerie Baumont, Marieke De Bruyne, Toon Rosseel, et al. 2020. “Unraveling Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss Using Long-Read Sequencing.” In Genetics of Ocular Development (GoOD) Meeting, Abstracts.
Chicago author-date (all authors)
Ascari, Giulia, Nanna D. Rendtorff, Julie Jacob, Julie De Zaeytijd, Valerie Baumont, Marieke De Bruyne, Toon Rosseel, Mattias Van Heetvelde, Tim De Pooter, Wouter De Coster, Peter De Rijk, Mojca Strazisar, Björn Menten, Lisbeth Tranebjærg, and Elfride De Baere. 2020. “Unraveling Complex Structural Variants of CEP78 Leading to Cone-Rod Dystrophy and Hearing Loss Using Long-Read Sequencing.” In Genetics of Ocular Development (GoOD) Meeting, Abstracts.
Vancouver
1.
Ascari G, Rendtorff ND, Jacob J, De Zaeytijd J, Baumont V, De Bruyne M, et al. Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing. In: Genetics of Ocular Development (GoOD) meeting, Abstracts. 2020.
IEEE
[1]
G. Ascari et al., “Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing,” in Genetics of Ocular Development (GoOD) meeting, Abstracts, Paris, France, 2020.
@inproceedings{8674031,
  author       = {{Ascari, Giulia and Rendtorff, Nanna D. and Jacob, Julie and De Zaeytijd, Julie and Baumont, Valerie and De Bruyne, Marieke and Rosseel, Toon and Van Heetvelde, Mattias and De Pooter, Tim and De Coster, Wouter and De Rijk, Peter and Strazisar, Mojca and Menten, Björn and Tranebjærg, Lisbeth and De Baere, Elfride}},
  booktitle    = {{Genetics of Ocular Development (GoOD) meeting, Abstracts}},
  language     = {{eng}},
  location     = {{Paris, France}},
  title        = {{Unraveling complex structural variants of CEP78 leading to cone-rod dystrophy and hearing loss using long-read sequencing}},
  url          = {{https://www.goodsoc.org/meetings/2020}},
  year         = {{2020}},
}