2 research outputs found
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
- Author
- A Itsara
- AJ Sharp
- B Teague
- BC Ballif
- Blake C Ballif
- Brian Teague
- C Shaw-Smith
- Can Alkan
- Catarina D Campbell
- CJ Shaw
- DA Koolen
- David C Schwartz
- DF Conrad
- DM Church
- DW Craig
- E Tuzun
- EE Eichler
- EG Bochukova
- ES Lander
- Evan E Eichler
- F Antonacci
- FD Hannes
- Francesca Antonacci
- H Kehrer-Sawatzki
- H Stefansson
- J Cheung
- J Martin
- JA Bailey
- JA Bailey
- JB Fan
- JD Parsons
- Jeffrey M Kidd
- Jill A Rosenfeld
- JM Kidd
- JR Lupski
- JR Lupski
- K Inoue
- LA Weiss
- Laura Vives
- Lisa G Shaffer
- LR Osborne
- M Cáceres
- M Laan
- MA Quail
- Maika Malig
- Mario Ventura
- MC Zody
- ME Johnson
- P Lichter
- P Stankiewicz
- R Ullmann
- RA Kumar
- Richard K Wilson
- S Giglio
- S Girirajan
- S Zhou
- S Zhou
- SA McCarroll
- Santhosh Girirajan
- SB Ng
- SW Scherer
- T Marques-Bonet
- Tina A Graves
- Tomas Marques-Bonet
- VG Cheung
- WJ Murphy
- Y Ji
- Z Jiang
- Z Jiang
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study