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
De Novo and Inherited Loss-of-Function Variants in TLK2: Cl..:
Reijnders, Margot RF
;
Miller, Kerry A
;
Alvi, Mohsan
...
qt9sv477rx. , 2018
Link:
https://escholarship.org/uc/item/9sv477rx
RT Journal T1
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt9sv477rx&Exemplar=1&LAN=DE A1 Reijnders, Margot RF A1 Miller, Kerry A A1 Alvi, Mohsan A1 Goos, Jacqueline AC A1 Lees, Melissa M A1 de Burca, Anna A1 Henderson, Alex A1 Kraus, Alison A1 Mikat, Barbara A1 de Vries, Bert BA A1 Isidor, Bertrand A1 Kerr, Bronwyn A1 Marcelis, Carlo A1 Schluth-Bolard, Caroline A1 Deshpande, Charu A1 Ruivenkamp, Claudia AL A1 Wieczorek, Dagmar A1 Study, The Deciphering Developmental Disorders A1 Baralle, Diana A1 Blair, Edward M A1 Engels, Hartmut A1 Lüdecke, Hermann-Josef A1 Eason, Jacqueline A1 Santen, Gijs WE A1 Clayton-Smith, Jill A1 Chandler, Kate A1 Tatton-Brown, Katrina A1 Payne, Katelyn A1 Helbig, Katherine A1 Radtke, Kelly A1 Nugent, Kimberly M A1 Cremer, Kirsten A1 Strom, Tim M A1 Bird, Lynne M A1 Sinnema, Margje A1 Bitner-Glindzicz, Maria A1 van Dooren, Marieke F A1 Alders, Marielle A1 Koopmans, Marije A1 Brick, Lauren A1 Kozenko, Mariya A1 Harline, Megan L A1 Klaassens, Merel A1 Steinraths, Michelle A1 Cooper, Nicola S A1 Edery, Patrick A1 Yap, Patrick A1 Terhal, Paulien A A1 van der Spek, Peter J A1 Lakeman, Phillis A1 Taylor, Rachel L A1 Littlejohn, Rebecca O A1 Pfundt, Rolph A1 Mercimek-Andrews, Saadet A1 Stegmann, Alexander PA A1 Kant, Sarina G A1 McLean, Scott A1 Joss, Shelagh A1 Swagemakers, Sigrid MA A1 Douzgou, Sofia A1 Wall, Steven A A1 Küry, Sébastien A1 Calpena, Eduardo A1 Koelling, Nils A1 McGowan, Simon J A1 Twigg, Stephen RF A1 Mathijssen, Irene MJ A1 Nellaker, Christoffer A1 Brunner, Han G A1 Wilkie, Andrew OM PB eScholarship, University of California YR 2018 K1 Biological Sciences K1 Bioinformatics and Computational Biology K1 Biomedical and Clinical Sciences K1 Genetics K1 Biotechnology K1 Brain Disorders K1 Human Genome K1 Neurosciences K1 Clinical Research K1 Aetiology K1 2.1 Biological and endogenous factors K1 Adolescent K1 Adult K1 Base Sequence K1 Cell Line K1 Child K1 Preschool K1 Facies K1 Female K1 Genetic Association Studies K1 Humans K1 Infant K1 Inheritance Patterns K1 Loss of Function Mutation K1 Male K1 Neurodevelopmental Disorders K1 Protein Kinases K1 RNA K1 Messenger K1 Translocation K1 Genetic K1 Young Adult K1 Deciphering Developmental Disorders Study K1 Tousled-like K1 facial averaging K1 haploinsufficiency K1 intellectual disability K1 kinase K1 Medical and Health Sciences K1 Genetics & Heredity K1 Health sciences JF qt9sv477rx LK http://dx.doi.org/https://escholarship.org/uc/item/9sv477rx DO https://escholarship.org/uc/item/9sv477rx SF ELIB - SuUB Bremen
Export
RefWorks (nur Desktop-Version!)
Flow
(Zuerst in
Flow
einloggen, dann importieren)