F. Hofstede
发表
J. Burgerhof,
C. Hollak,
N. Blau,
2013,
Orphanet Journal of Rare Diseases.
J. Abdenur,
M. Tassini,
N. Dorison,
2018,
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
A. Munnich,
C. Schwartz,
P. Pouwels,
2013,
Journal of Medical Genetics.
C. Hollak,
M. Heiner-Fokkema,
M. Vries,
2011,
Molecular genetics and metabolism.
J. Jans,
P. V. van Hasselt,
G. Visser,
2015,
PloS one.
C. Hollak,
F. Eyskens,
D. Cassiman,
2022,
Journal of inherited metabolic disease.
H. Blom,
Y. Chien,
W. Hwu,
2015,
Orphanet Journal of Rare Diseases.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2018,
Molecular genetics and metabolism.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2017,
Behavior Genetics.
M. Couce,
A. Chakrapani,
Á. García-Cazorla,
2016,
Orphanet Journal of Rare Diseases.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2016,
Journal of Inherited Metabolic Disease.
L. Sonneville,
C. Hollak,
S. Huijbregts,
2016
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Rebecca C. Spillmann,
J. Rosenfeld,
R. Pfundt,
2019,
American journal of human genetics.
E. Holme,
E. Schaftingen,
J. Smeitink,
2010,
Science.
E. Cuppen,
W. Kloosterman,
H. K. Ploos van Amstel,
2014,
American journal of medical genetics. Part A.
L. D. de Vries,
K. Lichtenbelt,
P. Lemmers,
2012,
Neuropediatrics.
S. Rajasekaran,
A. Rauch,
R. Kuzniecky,
2021,
American journal of medical genetics. Part A.
N. Verhoeven,
T. D. de Koning,
P. V. van Hasselt,
2011,
Pediatrics.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2015,
Molecular genetics and metabolism.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2013,
Molecular Genetics and Metabolism.
C. Hollak,
L. D. de Sonneville,
S. Huijbregts,
2017,
Neuropsychology.
L. Sonneville,
C. Hollak,
S. Huijbregts,
2017
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H. Maurice‐Stam,
M. Grootenhuis,
M. D. De Vries,
2013,
Molecular genetics and metabolism.
N. Verhoeven,
T. D. de Koning,
P. V. van Hasselt,
2011,
Pediatrics.
M. D. De Vries,
A. Bosch,
F. V. van Spronsen,
2016,
Orphanet Journal of Rare Diseases.
E. Christensen,
N. Dorison,
A. Lund,
2014,
Human mutation.
R. Pfundt,
F. Kortüm,
C. Gilissen,
2024,
American journal of human genetics.
B. D. de Vries,
A. V. D. van den Ouweland,
W. Hul,
1995,
American journal of human genetics.