I agree that this site is using cookies. You can find further informations
here
.
X
Login
Merkliste (
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
zur Desktop-Version
Toggle navigation
Merkliste
1 Ergebnisse
1
Table_2_Case report: Expanding the phenotype of FOXP1-relat..:
Carlo Alberto Cesaroni
;
Marzia Pollazzon
;
Cecilia Mancini
...
doi:10.3389/fneur.2023.1207176.s002. , 2023
Link:
https://doi.org/10.3389/fneur.2023.1207176.s002
RT Journal T1
Table_2_Case report: Expanding the phenotype of FOXP1-related intellectual disability syndrome and hyperkinetic movement disorder in differential diagnosis with epileptic seizures.docx
UL https://suche.suub.uni-bremen.de/peid=base-ftfrontimediafig:oai:figshare.com:article_23685891&Exemplar=1&LAN=DE A1 Carlo Alberto Cesaroni A1 Marzia Pollazzon A1 Cecilia Mancini A1 Susanna Rizzi A1 Camilla Cappelletti A1 Simone Pizzi A1 Daniele Frattini A1 Carlotta Spagnoli A1 Stefano Giuseppe Caraffi A1 Roberta Zuntini A1 Gabriele Trimarchi A1 Marcello Niceta A1 Francesca Clementina Radio A1 Marco Tartaglia A1 Livia Garavelli A1 Carlo Fusco YR 2023 K1 Neurology and Neuromuscular Diseases K1 Neurogenetics K1 autism K1 epilepsy K1 movement disorder K1 angiomas K1 choanal atresia K1 FOXP1 JF doi:10.3389/fneur.2023.1207176.s002 LK http://dx.doi.org/https://doi.org/10.3389/fneur.2023.1207176.s002 DO https://doi.org/10.3389/fneur.2023.1207176.s002 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)