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
Additional file 1 of Broadening the phenotype and genotype ..:
Mohammad-Reza Ghasemi
;
Sahand Tehrani Fateh
;
Aysan Moeinafshar
...
doi:10.6084/m9.figshare.25210684.v1. , 2024
Link:
https://doi.org/10.6084/m9.figshare.25210684.v1
RT Journal T1
Additional file 1 of Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review
UL https://suche.suub.uni-bremen.de/peid=base-ftgriffithunifig:oai:figshare.com:article_25210684&Exemplar=1&LAN=DE A1 Mohammad-Reza Ghasemi A1 Sahand Tehrani Fateh A1 Aysan Moeinafshar A1 Hossein Sadeghi A1 Parvaneh Karimzadeh A1 Reza Mirfakhraie A1 Mitra Rezaei A1 Farzad Hashemi-Gorji A1 Morteza Rezvani Kashani A1 Fatemehsadat Fazeli Bavandpour A1 Saman Bagheri A1 Parinaz Moghimi A1 Masoumeh Rostami A1 Rasoul Madannejad A1 Hassan Roudgari A1 Mohammad Miryounesi YR 2024 K1 Genetics K1 Pontocerebellar Hypoplasia K1 PCH K1 Whole exome sequencing K1 WES K1 Novel mutations K1 Novel clinical findings JF doi:10.6084/m9.figshare.25210684.v1 LK http://dx.doi.org/https://doi.org/10.6084/m9.figshare.25210684.v1 DO https://doi.org/10.6084/m9.figshare.25210684.v1 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)