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January 12, 2018SHILAP Revista de lepidopterologíaOpen Access

Cytogenomic identification and long-read single molecule real-time (SMRT) sequencing of a Bardet–Biedl Syndrome 9 (BBS9) deletion

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Authors

JRJennifer ReinerLPLaura Rosa PisaniWQWanqiong Qiao

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Reiner et al. (2018) studied this question.

synapsesocial.com/papers/69d6d87fa0177bf533ed933bhttps://doi.org/10.1038/s41525-017-0042-3
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Long-Read Single Molecule Real-Time Full Gene Sequencing of Cytochrome P450-2D62015 · 105 citations
  2. 2Bardet-Biedl syndrome in Denmark-report of 13 novel sequence variations in six genes2010 · 79 citations
  3. 3New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey1999 · 983 citations
  4. 4Knockdown of Bardet-Biedl Syndrome Gene BBS9/PTHB1 Leads to Cilia Defects2012 · 55 citations