Gretchen Foskett
发表
F. Alkuraya,
M. Salih,
P. Atwal,
2019,
Orphanet Journal of Rare Diseases.
W. Chan,
H. Prokisch,
F. Alkuraya,
2017,
Human mutation.
D. Stevenson,
Okmi Choi,
Lorna Tolentino,
2018,
Pediatric Neurology.