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 heterozygous mutation in GJB2 (Cx26F142L) associated with..:
Albuloushi, Ahmad
;
Lovgren, Marie‐Louise
;
Steel, Ainsley
...
Experimental Dermatology. 29 (2020) 10 - p. 970-979 , 2020
Link:
https://doi.org/10.1111/exd.14187
RT Journal T1
A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_exd.14187&Exemplar=1&LAN=DE A1 Albuloushi, Ahmad A1 Lovgren, Marie‐Louise A1 Steel, Ainsley A1 Yeoh, Yeelon A1 Waters, Alex A1 Zamiri, Mozheh A1 Martin, Patricia E. PB Wiley YR 2020 SN 0906-6705 SN 1600-0625 JF Experimental Dermatology VO 29 IS 10 SP 970 OP 979 LK http://dx.doi.org/https://doi.org/10.1111/exd.14187 DO https://doi.org/10.1111/exd.14187 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)