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
De Novo Missense Substitutions in the Gene Encoding CDK8, a..:
Calpena, E
;
Hervieu, A
;
Kaserer, T
...
American journal of human genetics, 2019, 104 (4), pp. 709 - 720. , 2019
Link:
https://repository.icr.ac.uk/handle/internal/3399
RT Journal T1
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder
UL https://suche.suub.uni-bremen.de/peid=base-ftinstcancerres:oai:repository.icr.ac.uk:internal_3399&Exemplar=1&LAN=DE A1 Calpena, E A1 Hervieu, A A1 Kaserer, T A1 Swagemakers, SMA A1 Goos, JAC A1 Popoola, O A1 Ortiz-Ruiz, MJ A1 Barbaro-Dieber, T A1 Bownass, L A1 Brilstra, EH A1 Brimble, E A1 Foulds, N A1 Grebe, TA A1 Harder, AVE A1 Lees, MM A1 Monaghan, KG A1 Newbury-Ecob, RA A1 Ong, K-R A1 Osio, D A1 Reynoso Santos, FJ A1 Ruzhnikov, MRZ A1 Telegrafi, A A1 van Binsbergen, E A1 van Dooren, MF A1 Deciphering Developmental Disorders Study A1 van der Spek, PJ A1 Blagg, J A1 Twigg, SRF A1 Mathijssen, IMJ A1 Clarke, PA A1 Wilkie, AOM PB CELL PRESS YR 2019 K1 Deciphering Developmental Disorders Study K1 Brain K1 Humans K1 Heart Defects K1 Congenital K1 Syndrome K1 Cyclin-Dependent Kinases K1 Developmental Disabilities K1 Phosphorylation K1 Heterozygote K1 Phenotype K1 Mutation K1 Missense K1 Child K1 Preschool K1 Infant K1 Female K1 Male K1 Cyclin C K1 Cyclin-Dependent Kinase 8 K1 Mediator Complex K1 Intellectual Disability K1 Exome JF American journal of human genetics, 2019, 104 (4), pp. 709 - 720 LK http://dx.doi.org/https://repository.icr.ac.uk/handle/internal/3399 DO https://repository.icr.ac.uk/handle/internal/3399 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)