I agree that this site is using cookies. You can find further informations
here
.
X
Login
My folder (
0
)
Home
About us
Home About us
Our history
Profile
Press & public relations
Friends
The library in figures
Exhibitions
Projects
Training, internships, careers
Films
Services & Information
Home Services & Information
Lending and interlibrary loans
Returns and renewals
Training and library tours
My Account
Library cards
New to the library?
Download Information
Opening hours
Learning spaces
PC, WLAN, copy, scan and print
Catalogs and collections
Home Catalogs and Collections
Rare books and manuscripts
Digital collections
Subject Areas
Our sites
Home Our sites
Central Library
Law Library (Juridicum)
BB Business and Economics (BB11)
BB Physics and Electrical Engineering
TB Engineering and Social Sciences
TB Economics and Nautical Sciences
TB Music
TB Art & Design
TB Bremerhaven
Contact the library
Home Contact the library
Staff Directory
Open access & publishing
Home Open access & publishing
Reference management: Citavi & RefWorks
Publishing documents
Open Access in Bremen
Show Desktop-Version
Toggle navigation
Verellen-Dumoulin, Christine
153
results:
Search for persons
X
Format
Online (153)
Mediatypes
Articles (Online) (63)
OpenAccess-fulltext (90)
Languages
english (139)
french (1)
Sorted by: Relevance
Sorted by: Year
?
1
Prevention of Neural Tube Defects in Europe: A Public Healt..:
Morris, Joan K.
;
Addor, Marie-Claude
;
Ballardini, Elisa
...
Frontiers in Pediatrics. 9 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
2
Epidemiology of septo-optic dysplasia with focus on prevale..:
Garne, Ester
;
Rissmann, Anke
;
Addor, Marie-Claude
...
European Journal of Medical Genetics. 61 (2018) 9 - p. 483-488 , 2018
Link:
https://doi.org/10.1016/..
?
3
Trends in congenital anomalies in Europe from 1980 to 2012:
Morris, Joan K.
;
Springett, Anna L.
;
Greenlees, Ruth
...
PLOS ONE. 13 (2018) 4 - p. e0194986 , 2018
Link:
https://doi.org/10.1371/..
?
4
Attentional impairments in Huntington's disease: A specific..:
Maurage, Pierre
;
Heeren, Alexandre
;
Lahaye, Magali
...
Neuropsychology. 31 (2017) 4 - p. 424-436 , 2017
Link:
https://doi.org/10.1037/..
?
5
HUWE1 variants cause dominant X-linked intellectual disabil..:
Moortgat, Stéphanie
;
Berland, Siren
;
Aukrust, Ingvild
...
European Journal of Human Genetics. 26 (2017) 1 - p. 64-74 , 2017
Link:
https://doi.org/10.1038/..
?
6
Dissociating emotional and cognitive empathy in pre-clinica..:
Maurage, Pierre
;
Lahaye, Magali
;
Grynberg, Delphine
...
Psychiatry Research. 237 (2016) - p. 103-108 , 2016
Link:
https://doi.org/10.1016/..
?
7
Clinical manifestations of intermediate allele carriers in ..:
Cubo, Esther
;
Ramos-Arroyo, María A.
;
Martinez-Horta, Saul
...
Neurology. 87 (2016) 6 - p. 571-578 , 2016
Link:
https://doi.org/10.1212/..
?
8
Long term trends in prevalence of neural tube defects in Eu..:
Khoshnood, Babak
;
Loane, Maria
;
de Walle, Hermien
...
BMJ: British Medical Journal. 351 (2015) - p. , 2015
Link:
https://www.jstor.org/st..
?
9
The Association of H1N1 Pandemic Influenza with Congenital ..:
Luteijn, Johannes Michiel
;
Addor, Marie-Claude
;
Arriola, Larraitz
...
Epidemiology. 26 (2015) 6 - p. 853-861 , 2015
Link:
https://www.jstor.org/st..
?
10
Holt Oram syndrome: a registry-based study in Europe:
Barisic, Ingeborg
;
Boban, Ljubica
;
Greenlees, Ruth
...
Orphanet Journal of Rare Diseases. 9 (2014) 1 - p. , 2014
Link:
https://doi.org/10.1186/..
?
11
Recent Decrease in the Prevalence of Congenital Heart Defec..:
Khoshnood, Babak
;
Loane, Maria
;
Garne, Ester
...
The Journal of Pediatrics. 162 (2013) 1 - p. 108-113.e2 , 2013
Link:
https://doi.org/10.1016/..
?
12
Deletion of KDM6A, a Histone Demethylase Interacting with M..:
Lederer, Damien
;
Grisart, Bernard
;
Digilio, Maria Cristina
...
The American Journal of Human Genetics. 90 (2012) 1 - p. 119-124 , 2012
Link:
https://doi.org/10.1016/..
?
13
Developmental delay and facial dysmorphism in a child with ..:
Moortgat, Stephanie
;
Verellen-Dumoulin, Christine
;
Maystadt, Isabelle
...
European Journal of Medical Genetics. 54 (2011) 2 - p. 177-180 , 2011
Link:
https://doi.org/10.1016/..
?
14
Mutations in FKBP10 cause recessive osteogenesis imperfecta..:
Kelley, Brian P
;
Malfait, Fransiska
;
Bonafe, Luisa
...
Journal of Bone and Mineral Research. 26 (2010) 3 - p. 666-672 , 2010
Link:
https://doi.org/10.1002/..
?
15
Prevalence and nonrandom distribution of exonic mutations i..:
de Lima, Renata L. L. Ferreira
;
Hoper, Sarah A.
;
Ghassibe, Michella
...
Genetics in Medicine. 11 (2009) 4 - p. 241-247 , 2009
Link:
https://doi.org/10.1097/..
1-15