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
Heterozygous nonsense ARX mutation in a family highlights t..:
Traversa, Alice
;
Marchionni, Enrica
;
Giovannetti, Agnese
...
info:eu-repo/semantics/altIdentifier/pmid/32519823. , 2020
Link:
http://hdl.handle.net/11573/1413909
RT Journal T1
Heterozygous nonsense ARX mutation in a family highlights the complexity of clinical and molecular diagnosis in case of chromosomal and single gene disorder co-inheritance
UL https://suche.suub.uni-bremen.de/peid=base-ftunivromairis:oai:iris.uniroma1.it:11573_1413909&Exemplar=1&LAN=DE A1 Traversa, Alice A1 Marchionni, Enrica A1 Giovannetti, Agnese A1 Genovesi, Maria L A1 Panzironi, Noemi A1 Margiotti, Katia A1 Napoli, Giulia A1 Piceci Sparascio, Francesca A1 De Luca, Alessandro A1 Petrizzelli, Francesco A1 Carella, Massimo A1 Cardona, Francesco A1 Bernardo, Silvia A1 Manganaro, Lucia A1 Mazza, Tommaso A1 Pizzuti, Antonio A1 Caputo, Viviana YR 2020 K1 ARX K1 17q12 duplication syndrome K1 array-CGH K1 clinical exome sequencing K1 corpus callosum K1 dual diagnosis JF info:eu-repo/semantics/altIdentifier/pmid/32519823 LK http://hdl.handle.net/11573/1413909 DO http://hdl.handle.net/11573/1413909 SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)