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The clinical use of exome sequencing to diagnose PCD patients

Lore Pottie (UGent) , Sofie Symoens (UGent) , Elfride De Baere (UGent) and Kathleen Claes (UGent)
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Citation

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

MLA
Pottie, Lore, et al. “The Clinical Use of Exome Sequencing to Diagnose PCD Patients.” EUROPEAN JOURNAL OF HUMAN GENETICS, vol. 32, no. Supplement 1, 2024, pp. 385–385.
APA
Pottie, L., Symoens, S., De Baere, E., & Claes, K. (2024). The clinical use of exome sequencing to diagnose PCD patients. EUROPEAN JOURNAL OF HUMAN GENETICS, 32(Supplement 1), 385–385.
Chicago author-date
Pottie, Lore, Sofie Symoens, Elfride De Baere, and Kathleen Claes. 2024. “The Clinical Use of Exome Sequencing to Diagnose PCD Patients.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 32:385–385.
Chicago author-date (all authors)
Pottie, Lore, Sofie Symoens, Elfride De Baere, and Kathleen Claes. 2024. “The Clinical Use of Exome Sequencing to Diagnose PCD Patients.” In EUROPEAN JOURNAL OF HUMAN GENETICS, 32:385–385.
Vancouver
1.
Pottie L, Symoens S, De Baere E, Claes K. The clinical use of exome sequencing to diagnose PCD patients. In: EUROPEAN JOURNAL OF HUMAN GENETICS. 2024. p. 385–385.
IEEE
[1]
L. Pottie, S. Symoens, E. De Baere, and K. Claes, “The clinical use of exome sequencing to diagnose PCD patients,” in EUROPEAN JOURNAL OF HUMAN GENETICS, Glasgow, Scotland, UK, 2024, vol. 32, no. Supplement 1, pp. 385–385.
@inproceedings{01HTY9A9DKQJSAZVHPWXJZ4SBT,
  articleno    = {{P04.007.C}},
  author       = {{Pottie, Lore and Symoens, Sofie and De Baere, Elfride and Claes, Kathleen}},
  booktitle    = {{EUROPEAN JOURNAL OF HUMAN GENETICS}},
  issn         = {{1018-4813}},
  language     = {{eng}},
  location     = {{Glasgow, Scotland, UK}},
  number       = {{Supplement 1}},
  pages        = {{P04.007.C:385--P04.007.C:385}},
  title        = {{The clinical use of exome sequencing to diagnose PCD patients}},
  volume       = {{32}},
  year         = {{2024}},
}

Web of Science
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