K. Bjørgo
发表
Alexander Münchau,
Caroline Hallam,
Andrea Ciarmiello,
2011,
PLoS currents.
Enrico Amico,
Philippe Allain,
Mark Mühlau,
2017,
The Lancet. Neurology.
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin‐binding dynamics
F. Cardarelli,
A. Renieri,
F. Mari,
2012,
Clinical genetics.
D. Misceo,
M. Rocchi,
E. Ormerod,
2008,
American journal of medical genetics. Part A.
Juan I. Young,
M. Tekin,
F. Brancati,
2015,
Human Genetics.
Juan I. Young,
M. Tekin,
F. Brancati,
2015,
Human Genetics.
S. Ferdinandusse,
H. Waterham,
K. Falkenberg,
2017,
Molecular genetics and metabolism.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
William E. Byrd,
Mercedes E. Alejandro,
Mahshid S. Azamian,
2021,
Genetics in Medicine.
Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations
William E. Byrd,
Gabor T. Marth,
David R. Murdock,
2021,
Genetics in Medicine.
O. Rødningen,
J. Andresen,
K. Bjørgo,
2017,
Journal of Medical Case Reports.
O. Rødningen,
S. B. Helverschou,
A. Kildahl,
2018
.
T. Holmøy,
P. Roos,
K. Bjørgo,
2007,
European Neurology.
J. Schiefer,
R. Barker,
R. Reilmann,
2011,
PLoS currents.
G. Tjønnfjord,
K. Bjørgo,
O. Kildahl‐Andersen,
2022,
BMJ Case Reports.
Nurit Assia Batzir,
J. Schuurs-Hoeijmakers,
R. Pfundt,
2024,
American journal of human genetics.