Smith, Amanda C
18748  results:
Search for persons X
?
5

A family segregating lethal neonatal coenzyme Q10 deficienc..:

Smith, Amanda C. ; Ito, Yoko ; Ahmed, Afsana...
Journal of Inherited Metabolic Disease.  41 (2018)  4 - p. 719-729 , 2018
 
?
6

Fragile X testing as a second-tier test:

Hartley, Taila ; Potter, Ryan ; Badalato, Lauren...
Genetics in Medicine.  19 (2017)  12 - p. 1380 , 2017
 
?
8

Neuropathologic Features of Pontocerebellar Hypoplasia Type..:

Joseph, Jeffrey T. ; Innes, A. Micheil ; Smith, Amanda C....
Journal of Neuropathology & Experimental Neurology.  73 (2014)  11 - p. 1009-1025 , 2014
 
?
10

Mutations in PIK3R1 Cause SHORT Syndrome:

Dyment, David A. ; Smith, Amanda C. ; Alcantara, Diana...
The American Journal of Human Genetics.  93 (2013)  1 - p. 158-166 , 2013
 
?
 
1-15