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
Case report: Extending the spectrum of clinical and molecul..:
Alexandra Garza Flores
;
Ida Nordgren
;
Maria Pettersson
...
https://www.frontiersin.org/articles/10.3389/fgene.2023.1174046/full. , 2023
Link:
https://doi.org/10.3389/fgene.2023.1174046
RT Journal T1
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftdoajarticles:oai:doaj.org_article:4c781b29b14b4f2ca44d5bf090231ae4&Exemplar=1&LAN=DE A1 Alexandra Garza Flores A1 Ida Nordgren A1 Maria Pettersson A1 Dora Dias-Santagata A1 Daniel Nilsson A1 Anna Hammarsjö A1 Anna Lindstrand A1 Dominyka Batkovskyte A1 Janey Wiggs A1 David S. Walton A1 Paula Goldenberg A1 Jesper Eisfeldt A1 Angela E. Lin A1 Ralph S. Lachman A1 Gen Nishimura A1 Giedre Grigelioniene PB Frontiers Media S.A. YR 2023 K1 FOXC1 K1 Axenfeld-Rieger Syndrome K1 De Hauwere Syndrome K1 skeletal anomalies K1 genome sequencing K1 case report K1 Genetics K1 QH426-470 JF https://www.frontiersin.org/articles/10.3389/fgene.2023.1174046/full LK http://dx.doi.org/https://doi.org/10.3389/fgene.2023.1174046 DO https://doi.org/10.3389/fgene.2023.1174046 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)