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
A Novel Heterozygous De Novo MORC2 Missense Variant Causes ..:
Arbide, Daniel
;
Elkhateeb, Nour
;
Goljan, Ewa
...
Case Reports in Genetics. 2024 (2024) - p. 1-5 , 2024
Link:
https://doi.org/10.1155/2024/5906936
RT Journal T1
A Novel Heterozygous De Novo MORC2 Missense Variant Causes an Early Onset and Severe Neurodevelopmental Disorder
UL https://suche.suub.uni-bremen.de/peid=cr-10.1155_2024_5906936&Exemplar=1&LAN=DE A1 Arbide, Daniel A1 Elkhateeb, Nour A1 Goljan, Ewa A1 Gonzalez, Carolina Perez A1 Maw, Anna A1 Park, Soo-Mi A1 Mittal, Balraj PB Hindawi Limited YR 2024 SN 2090-6552 SN 2090-6544 JF Case Reports in Genetics VO 2024 SP 1 OP 5 LK http://dx.doi.org/https://doi.org/10.1155/2024/5906936 DO https://doi.org/10.1155/2024/5906936 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)