G. Mitchell
发表
R. Tanguay,
P. Russo,
G. Mitchell,
2001,
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.
Isabelle De Bie,
S. Nizard,
G. Mitchell,
2009,
Prenatal diagnosis.
E. Rossignol,
M. Brivet,
Ivan Shelihan,
2021,
JIMD reports.
P. Waters,
Shupei Wang,
Gongshe Yang,
2021,
Molecular genetics and metabolism.
J. Soucy,
B. Ellezam,
M. Harissi-Dagher,
2021,
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.
B. Hartmann,
P. Huppke,
C. Pérez-Cerdá,
2017,
Clinical genetics.
Mingzhou Li,
L. Bai,
Enqi Liu,
2021,
PLoS genetics.
T. Fukao,
H. Shintaku,
H. Watanabe,
1998,
Human mutation.
G. Mitchell,
D. Cyr,
L. Hermo,
2008,
Molecular reproduction and development.
J. Gauthier,
G. Horvath,
J. Soucy,
2022,
JIMD reports.
G. Mitchell,
B. Robinson,
J. Cameron,
2006,
European Journal of Pediatrics.
A. Pshezhetsky,
M. Elsliger,
M. Potier,
1998,
Human mutation.
G. Mitchell,
S. Chouinard,
T. Fukao,
2013,
Movement disorders : official journal of the Movement Disorder Society.
A. Montpetit,
I. Thiffault,
B. Brais,
2013,
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
J. Ragoussis,
A. Montpetit,
C. Carvalho,
2023,
Haemophilia : the official journal of the World Federation of Hemophilia.
J. Michaud,
G. Mitchell,
L. Garel,
2006,
American journal of medical genetics. Part A.
Lois E. H. Smith,
C. Clish,
G. Andelfinger,
2022,
JCI insight.
S. Jacobson,
G. Fishman,
J. Duncan,
2011,
Human mutation.
J. Michaud,
G. Mitchell,
J. Himms-Hagen,
2001,
Human molecular genetics.
B. Maranda,
G. Mitchell,
B. Robinson,
2008,
Neuropediatrics.