Search

Author/Creator Griffith, Christopher

1. Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss. Issue 12 (2nd August 2022)

Authors:
Chen, Robert; Diaz‐Miranda, Maria Alejandra; Aref‐Eshghi, Erfan; Hartman, Tiffiney R.; Griffith, Christopher; Morrison, Jennifer L.; Wheeler, Patricia G.; Torti, Erin; Richard, Gabriele; Kenna, Margaret; Dechene, Elizabeth T.; Spinner, Nancy B.; Bai, Renkui; Conlin, Laura K.; Krantz, Ian D.; Amr,...
Journal:
Human mutation
Issue:
Volume 43:Issue 12(2022)
Page Start:
1837
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic Movements. (February 2021)

Authors:
Abdelmoumen, Imane; Jimenez, Sandra; Valencia, Ignacio; Melvin, Joseph; Legido, Agustin; Diaz-Diaz, Mayela M.; Griffith, Christopher; Massingham, Lauren J.; Yelton, Melissa; Rodríguez-Hernández, Janice; Schnur, Rhonda E.; Walsh, Laurence E.; Cristancho, Ana G.; Bergqvist, Christina A.; McWalter, ...
Journal:
Journal of child neurology
Issue:
Volume 36:Number 2(2021)
Page Start:
93
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. TORS elective lingual tonsillectomy has less acute morbidity than therapeutic base of tongue TORS. (June 2021)

Authors:
Patel, Mihir R.; Ottenstein, Lauren; Ryan, Martha; Farrell, Annie; Studer, Matthew; Baddour, H. Michael; Magliocca, Kelly; Griffith, Christopher; Stokes, William; Switchenko, Jeffrey; Aiken, Ashley; El-Deiry, Mark; Solares, C. Arturo; Steuer, Conor; Saba, Nabil; Beitler, Jonathan
Journal:
Oral oncology
Issue:
Volume 117(2021)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: A previously undescribed syndrome?. (23rd February 2015)

Authors:
Jackson, Jessica; Delk, Paula; Farrow, Emily; Griffith, Christopher; Lah, Melissa; Weaver, David D.
Journal:
American journal of medical genetics
Issue:
Volume 167:Number 4(2015:Apr.)
Page Start:
683
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗