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
Biallelic variants in ZNF142 lead to a syndromic neurodevel..:
Christensen, Maria B
;
Levy, Amanda M
;
Mohammadi, Nazanin A
...
https://discovery.ucl.ac.uk/id/eprint/10149455/3/Magrinelli_Clinical%20Genetics%20-%202022%20-%20Christensen%20-%20Biallelic%20variants%20in%20ZNF142%20lead%20to%20a%20syndromic%20neurodevelopmental%20disorder.pdf. , 2022
Link:
https://discovery.ucl.ac.uk/id/eprint/10149455/3/Magri..
RT Journal T1
Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder
UL https://suche.suub.uni-bremen.de/peid=base-ftucl:oai:eprints.ucl.ac.uk.OAI2:10149455&Exemplar=1&LAN=DE A1 Christensen, Maria B A1 Levy, Amanda M A1 Mohammadi, Nazanin A A1 Niceta, Marcello A1 Kaiyrzhanov, Rauan A1 Dentici, Maria Lisa A1 Alam, Chadi Al A1 Alesi, Viola A1 Benoit, Valérie A1 Bhatia, Kailash P A1 Bierhals, Tatjana A1 Boßelmann, Christian M A1 Buratti, Julien A1 Callewaert, Bert A1 Ceulemans, Berten A1 Charles, Perrine A1 De Wachter, Matthias A1 Dehghani, Mohammadreza A1 D'haenens, Erika A1 Doco-Fenzy, Martine A1 Geßner, Michaela A1 Gobert, Cyrielle A1 Guliyeva, Ulviyya A1 Haack, Tobias B A1 Hammer, Trine B A1 Heinrich, Tilman A1 Hempel, Maja A1 Herget, Theresia A1 Hoffmann, Ute A1 Horvath, Judit A1 Houlden, Henry A1 Keren, Boris A1 Kresge, Christina A1 Kumps, Candy A1 Lederer, Damien A1 Lermine, Alban A1 Magrinelli, Francesca A1 Maroofian, Reza A1 Mehrjardi, Mohammad Yahya Vahidi A1 Moudi, Mahdiyeh A1 Müller, Amelie J A1 Oostra, Anna J A1 Pletcher, Beth A A1 Ros-Pardo, David A1 Samarasekera, Shanika A1 Tartaglia, Marco A1 Van Schil, Kristof A1 Vogt, Julie A1 Wassmer, Evangeline A1 Winkelmann, Juliane A1 Zaki, Maha S A1 Zech, Michael A1 Lerche, Holger A1 Radio, Francesca Clementina A1 Gomez-Puertas, Paulino A1 Møller, Rikke S A1 Tümer, Zeynep PB Wiley YR 2022 K1 ZNF142 K1 epilepsy K1 intellectual disability K1 language impairement K1 movement disorder K1 neurodevelopmental disorder JF https://discovery.ucl.ac.uk/id/eprint/10149455/3/Magrinelli_Clinical%20Genetics%20-%202022%20-%20Christensen%20-%20Biallelic%20variants%20in%20ZNF142%20lead%20to%20a%20syndromic%20neurodevelopmental%20disorder.pdf LK http://dx.doi.org/https://discovery.ucl.ac.uk/id/eprint/10149455/3/Magrinelli_Clinical%20Genetics%20-%202022%20-%20Christensen%20-%20Biallelic%20variants%20in%20ZNF142%20lead%20to%20a%20syndromic%20neurodevelopmental%20disorder.pdf DO https://discovery.ucl.ac.uk/id/eprint/10149455/3/Magrinelli_Clinical%20Genetics%20-%202022%20-%20Christensen%20-%20Biallelic%20variants%20in%20ZNF142%20lead%20to%20a%20syndromic%20neurodevelopmental%20disorder.pdf SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)