Search

Author/Creator Gurnett, Christina A.

1. De novo KCNA1 variants in the PVP motif cause infantile epileptic encephalopathy and cognitive impairment similar to recurrent KCNA2 variants. Issue 8 (28th July 2018)

Authors:
Rogers, Amanda; Golumbek, Paul; Cellini, Elena; Doccini, Viola; Guerrini, Renzo; Wallgren‐Pettersson, Carina; Thuresson, Ann‐Charlotte; Gurnett, Christina A.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 8(2018)
Page Start:
1748
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Design and descriptive data of the randomized Clubfoot Foot Abduction Brace Length of Treatment Study (FAB24). Issue 2 (March 2017)

Authors:
Dobbs, Matthew B.; Frick, Steven L.; Mosca, Vincent S.; Raney, Ellen; VanBosse, Harold J.; Lerman, Joel A.; Talwalkar, Vishwas R.; Steger-May, Karen; Gurnett, Christina A.
Journal:
Journal of pediatric orthopedics
Issue:
Volume 26:Issue 2(2017)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. Summary of the first inaugural joint meeting of the International Consortium for scoliosis genetics and the International Consortium for vertebral anomalies and scoliosis, March 16–18, 2017, Dallas, Texas. Issue 1 (21st November 2017)

Authors:
Giampietro, Philip F.; Pourquie, Olivier; Raggio, Cathy; Ikegawa, Shiro; Turnpenny, Peter D.; Gray, Ryan; Dunwoodie, Sally L.; Gurnett, Christina A.; Alman, Benjamin; Cheung, Kenneth; Kusumi, Kenro; Hadley‐Miller, Nancy; Wise, Carol A.
Journal:
American journal of medical genetics
Issue:
Volume 176:Issue 1(2018)
Page Start:
253
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗