Showing 1–6 of 6 results
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Research | | Open
Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease
- Andrew M. Gross
- , Subramanian S. Ajay
- , Vani Rajan
- , Carolyn Brown
- , Krista Bluske
- , Nicole J. Burns
- , Aditi Chawla
- , Alison J. Coffey
- , Alka Malhotra
- , Alicia Scocchia
- , Erin Thorpe
- , Natasa Dzidic
- , Karine Hovanes
- , Trilochan Sahoo
- , Egor Dolzhenko
- , Bryan Lajoie
- , Amirah Khouzam
- , Shimul Chowdhury
- , John Belmont
- , Eric Roller
- , Sergii Ivakhno
- , Stephen Tanner
- , Julia McEachern
- , Tina Hambuch
- , Michael Eberle
- , R. Tanner Hagelstrom
- , David R. Bentley
- , Denise L. Perry
- & Ryan J. Taft
