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
Genotype–Phenotype Correlations in Children with HHT:
Kilian, Alexandra
;
Latino, Giuseppe A
;
White, Andrew J
...
qt1c81h48r. , 2020
Link:
https://escholarship.org/uc/item/1c81h48r
RT Journal T1
Genotype–Phenotype Correlations in Children with HHT
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt1c81h48r&Exemplar=1&LAN=DE A1 Kilian, Alexandra A1 Latino, Giuseppe A A1 White, Andrew J A1 Clark, Dewi A1 Chakinala, Murali M A1 Ratjen, Felix A1 McDonald, Jamie A1 Whitehead, Kevin J A1 Gossage, James R A1 Lin, Doris A1 Henderson, Katharine A1 Pollak, Jeffrey A1 McWilliams, Justin P A1 Kim, Helen A1 Lawton, Michael T A1 Faughnan, Marie E PB eScholarship, University of California YR 2020 K1 Hematology K1 Clinical Research K1 Congenital Structural Anomalies K1 Lung K1 Orphan Drug K1 Pediatric K1 Rare Diseases K1 Genetics K1 Neurosciences K1 2.1 Biological and endogenous factors K1 Aetiology K1 Hereditary hemorrhagic telangiectasia K1 pediatrics K1 genotype-phenotype correlation K1 arteriovenous malformation K1 ENG K1 ACVRL1 K1 SMAD4 K1 the Brain Vascular Malformation Consortium HHT Investigator Group K1 genotype–phenotype correlation K1 Clinical Sciences JF qt1c81h48r LK http://dx.doi.org/https://escholarship.org/uc/item/1c81h48r DO https://escholarship.org/uc/item/1c81h48r SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)