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
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Sy..:
Capri, Yline
;
Flex, Elisabetta
;
Krumbach, Oliver HF
...
qt23r6955g. , 2019
Link:
https://escholarship.org/uc/item/23r6955g
RT Journal T1
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt23r6955g&Exemplar=1&LAN=DE A1 Capri, Yline A1 Flex, Elisabetta A1 Krumbach, Oliver HF A1 Carpentieri, Giovanna A1 Cecchetti, Serena A1 Lißewski, Christina A1 Rezaei Adariani, Soheila A1 Schanze, Denny A1 Brinkmann, Julia A1 Piard, Juliette A1 Pantaleoni, Francesca A1 Lepri, Francesca R A1 Goh, Elaine Suk-Ying A1 Chong, Karen A1 Stieglitz, Elliot A1 Meyer, Julia A1 Kuechler, Alma A1 Bramswig, Nuria C A1 Sacharow, Stephanie A1 Strullu, Marion A1 Vial, Yoann A1 Vignal, Cédric A1 Kensah, George A1 Cuturilo, Goran A1 Kazemein Jasemi, Neda S A1 Dvorsky, Radovan A1 Monaghan, Kristin G A1 Vincent, Lisa M A1 Cavé, Hélène A1 Verloes, Alain A1 Ahmadian, Mohammad R A1 Tartaglia, Marco A1 Zenker, Martin PB eScholarship, University of California YR 2019 K1 Biochemistry and Cell Biology K1 Bioinformatics and Computational Biology K1 Biomedical and Clinical Sciences K1 Biological Sciences K1 Genetics K1 Intellectual and Developmental Disabilities (IDD) K1 Pediatric K1 Brain Disorders K1 Congenital Structural Anomalies K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adult K1 Child K1 Female K1 Gain of Function Mutation K1 Genetic Association Studies K1 Guanosine Triphosphate K1 HEK293 Cells K1 Humans K1 Infant K1 Newborn K1 Male K1 Membrane Proteins K1 Monomeric GTP-Binding Proteins K1 Noonan Syndrome K1 Pedigree K1 Protein Conformation K1 MAPK K1 RAS K1 RASopathies K1 RRAS2 K1 Medical and Health Sciences K1 Genetics & Heredity K1 Health sciences JF qt23r6955g LK http://dx.doi.org/https://escholarship.org/uc/item/23r6955g DO https://escholarship.org/uc/item/23r6955g SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)