J. Bergman
发表
E. Otten,
J. Verheij,
H. D. De Walle,
2016,
Reproductive toxicology.
Tania A Desrosiers,
Carissa M Rocheleau,
H. Boezen,
2020,
Occupational and Environmental Medicine.
Hao Wang,
B. Wilffert,
T. Plösch,
2014,
Pharmacogenomics.
J. G. Post,
G. Pals,
M. Berg,
2008,
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation.
A. Pierini,
D. Tucker,
Shiliang Liu,
2019,
BMJ Open.
J. Cobben,
R. Oostra,
J. Bergman,
2016,
Birth defects research. Part A, Clinical and molecular teratology.
M. Loane,
E. Garne,
A. Neville,
2021,
Reproductive toxicology.
W. D. den Dunnen,
J. P. van Tintelen,
A. V. van Essen,
2007,
European journal of medical genetics.
J. Bergman,
K. Bouman,
J. Erwich,
2021,
Paediatric and perinatal epidemiology.
L. Hoefsloot,
Anna M Koszucka,
M. Elbracht,
2010,
Human molecular genetics.
Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control Study
L. Meiners,
J. Bergman,
C. van Ravenswaaij-Arts,
2018,
American Journal of Neuroradiology.
C. V. van Ravenswaaij-Arts,
J. Bergman,
E. Scholte,
2009,
Journal of developmental and physical disabilities.
L. Hoefsloot,
C. V. van Ravenswaaij-Arts,
M. Jongmans,
2008,
European journal of medical genetics.
M. Loane,
M. Haeusler,
A. Latos-Bieleńska,
2019,
Pediatric Research.
M. Loane,
E. Garne,
A. Neville,
2017,
Drug Safety.
F. Bianchi,
E. Garne,
M. Haeusler,
2019,
Neuroepidemiology.
M. Hadders‐Algra,
M. Haadsma,
H. Groen,
2015,
Fertility and sterility.
E. Garne,
M. Haeusler,
E. Calzolari,
2014,
Orphanet Journal of Rare Diseases.
M. Loane,
E. Garne,
M. Haeusler,
2015,
American journal of medical genetics. Part A.
M. Loane,
S. Bianca,
R. Tenconi,
2013,
American journal of medical genetics. Part A.
M. Loane,
E. Garne,
A. Neville,
2018,
PloS one.
E. Hak,
B. Wilffert,
H. D. De Walle,
2017,
BMC Pregnancy and Childbirth.
M. Loane,
S. Bianca,
E. Garne,
2014,
European Journal of Human Genetics.
A. Pierini,
M. Morgan,
E. Szabová,
2022,
American journal of perinatology.
A. Pierini,
M. Morgan,
E. Szabová,
2020,
Birth defects research.
Hao Wang,
E. Hak,
B. Wilffert,
2015,
Drug Safety.
M. Swertz,
L. Hoefsloot,
R. Hofstra,
2012,
Human mutation.
R. Hofstra,
L. Hoefsloot,
R. Hofstra,
2011,
Journal of Medical Genetics.
L. Hoefsloot,
R. Hofstra,
C. V. van Ravenswaaij-Arts,
2012,
Human mutation.
I. V. van Rooij,
J. Giltay,
N. Roeleveld,
2020,
Birth defects research.
I. V. van Rooij,
M. Loane,
A. Latos-Bieleńska,
2020,
Birth defects research.
A. Latos-Bieleńska,
C. Cavero-Carbonell,
A. Materna-Kiryluk,
2018,
European journal of medical genetics.
K. Heimdal,
R. Hennekam,
L. Hoefsloot,
2013,
Circulation. Cardiovascular genetics.
Ginette M Ecury-Goossen,
M. Mannens,
J. Bergman,
2023,
Birth defects research.
B. Wilffert,
H. Groen,
J. Bergman,
2016,
International journal of molecular sciences.
A J Agopian,
F. Bianchi,
A. Pierini,
2019,
European urology.
B. Wilffert,
H. Groen,
J. Bergman,
2017,
CNS Drugs.
B. Wilffert,
H. Groen,
J. Bergman,
2017
.
L. Hoefsloot,
L. Meiners,
C. V. van Ravenswaaij-Arts,
2011,
The Journal of pediatrics.
C. K. van der Sluis,
P. Rump,
Katharina Löhner,
2020,
American journal of medical genetics. Part A.
M. Loane,
S. Bianca,
R. Tenconi,
2013
.
M. Vrijheid,
M. Loane,
A. Neville,
2015,
World Journal of Urology.
L. Hoefsloot,
B. Wolffenbuttel,
C. V. van Ravenswaaij-Arts,
2012,
The Journal of clinical endocrinology and metabolism.
J. van Reeuwijk,
L. Hoefsloot,
H. van Bokhoven,
2010,
Brain : a journal of neurology.
M. Loane,
E. Garne,
M. Haeusler,
2014,
European Journal of Human Genetics.
Pieter U Dijkstra,
Corry K van der Sluis,
C. K. van der Sluis,
2013,
BMC Musculoskeletal Disorders.
E. Hak,
B. Wilffert,
H. Groen,
2017,
Pharmacoepidemiology and drug safety.
K. Steel,
C. V. van Ravenswaaij-Arts,
J. Bergman,
2009,
European Journal of Human Genetics.
R. Vermeulen,
H. Boezen,
H. Kromhout,
2016,
Environmental Health.
F. Bianchi,
E. Garne,
M. Haeusler,
2014,
Birth defects research. Part A, Clinical and molecular teratology.
A. Pierini,
M. Morgan,
E. Szabová,
2022,
Birth defects research.
H. Boezen,
H. Kromhout,
M. van Tongeren,
2021,
Human reproduction.
C. Bilardo,
J. Bergman,
M. Bakker,
2018,
Prenatal diagnosis.
H. Boezen,
N. Smidt,
H. Kromhout,
2019,
Human reproduction.
M. Loane,
M. Swertz,
A. Neville,
2021,
Clinical pharmacology and therapeutics.
A. Pierini,
M. Morgan,
E. Szabová,
2021,
Birth defects research.
E. Garne,
M. Haeusler,
A. Neville,
2019,
Archives of Disease in Childhood.
E. Garne,
M. Haeusler,
A. Neville,
2018,
European journal of medical genetics.
M. Loane,
E. Garne,
A. Neville,
2016,
British Medical Journal.
K. Heimdal,
R. Hennekam,
C. Rustad,
2014
.
E. Hak,
B. Wilffert,
H. Groen,
2017,
Pharmacogenomics.
M. P. van den Berg,
D. Halley,
J. P. van Tintelen,
2014,
American journal of medical genetics. Part A.
M. Loane,
M. Haeusler,
A. Latos-Bieleńska,
2022,
American journal of medical genetics. Part A.
R. Vermeulen,
H. Boezen,
H. Kromhout,
2020,
Scandinavian journal of work, environment & health.
E. Garne,
M. Haeusler,
A. Neville,
2022,
Birth defects research.
E. Hak,
B. Wilffert,
H. Groen,
2017,
PloS one.
F. Bianchi,
E. Garne,
M. Haeusler,
2019,
American journal of medical genetics. Part A.
B. Wilffert,
H. Groen,
J. Bergman,
2016
.
B. Wilffert,
H. Groen,
J. Bergman,
2016,
International journal of molecular sciences.
E. V. van Puijenbroek,
R. Dolhain,
J. Bergman,
2022,
British journal of clinical pharmacology.
L. Hoefsloot,
W. Crowley,
T. Ogata,
2009,
Clinical genetics.
R. Snijders,
C. Bilardo,
H. D. De Walle,
2014,
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.
E. Hak,
B. Wilffert,
H. Groen,
2017,
PloS one.
F. Bianchi,
E. Garne,
M. Haeusler,
2014,
Birth defects research. Part A, Clinical and molecular teratology.
J. Cobben,
R. Oostra,
J. Bergman,
2016,
Birth defects research. Clinical and molecular teratology.
E. Garne,
A. Neville,
A. Pierini,
2019
.