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
CHEDDAsyndrome is an underrecognized neurodevelopmental dis..:
Palmer, Elizabeth E.
;
Whitton, Chloe
;
Hashem, Mais O.
...
Clinical Genetics. 100 (2021) 4 - p. 468-477 , 2021
Link:
https://doi.org/10.1111/cge.14022
RT Journal T1
CHEDDAsyndrome is an underrecognized neurodevelopmental disorder with a highly restrictedATN1mutation spectrum
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14022&Exemplar=1&LAN=DE A1 Palmer, Elizabeth E. A1 Whitton, Chloe A1 Hashem, Mais O. A1 Clark, Robin D. A1 Ramanathan, Subhadra A1 Starr, Lois J. A1 Velasco, Danita A1 De Dios, John Karl A1 Singh, Emily A1 Cormier‐Daire, Valerie A1 Chopra, Maya A1 Rodan, Lance H. A1 Nellaker, Christoffer A1 Lakhani, Shenela A1 Mallack, Eric J. A1 Panzer, Karin A1 Sidhu, Alpa A1 Wentzensen, Ingrid M. A1 Lacombe, Didier A1 Michaud, Vincent A1 Alkuraya, Fowzan S. PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 100 IS 4 SP 468 OP 477 LK http://dx.doi.org/https://doi.org/10.1111/cge.14022 DO https://doi.org/10.1111/cge.14022 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)