Titel

Merkliste
1 Ergebnisse

De Novo and Inherited Loss-of-Function Variants in TLK2: Cl..:

Reijnders, MRF ; Miller, KA ; Alvi, M...
https://openaccess.sgul.ac.uk/id/eprint/109920/1/1-s2.0-S0002929718301617-main.pdf. , 2018

Link: https://openaccess.sgul.ac.uk/id/eprint/109920/

RT Journal
T1 <Title>De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftstgeorgesuniv:oai:openaccess.sgul.ac.uk:109920&Exemplar=1&LAN=DE
				
A1 Reijnders, MRF
A1 Miller, KA
A1 Alvi, M
A1 Goos, JAC
A1 Lees, MM
A1 de Burca, A
A1 Henderson, A
A1 Kraus, A
A1 Mikat, B
A1 de Vries, BBA
A1 Isidor, B
A1 Kerr, B
A1 Marcelis, C
A1 Schluth-Bolard, C
A1 Deshpande, C
A1 Ruivenkamp, CAL
A1 Wieczorek, D
A1 Deciphering Developmental Disorders Study
A1 Baralle, D
A1 Blair, EM
A1 Engels, H
A1 Lüdecke, H-J
A1 Eason, J
A1 Santen, GWE
A1 Clayton-Smith, J
A1 Chandler, K
A1 Tatton-Brown, K
A1 Payne, K
A1 Helbig, K
A1 Radtke, K
A1 Nugent, KM
A1 Cremer, K
A1 Strom, TM
A1 Bird, LM
A1 Sinnema, M
A1 Bitner-Glindzicz, M
A1 van Dooren, MF
A1 Alders, M
A1 Koopmans, M
A1 Brick, L
A1 Kozenko, M
A1 Harline, ML
A1 Klaassens, M
A1 Steinraths, M
A1 Cooper, NS
A1 Edery, P
A1 Yap, P
A1 Terhal, PA
A1 van der Spek, PJ
A1 Lakeman, P
A1 Taylor, RL
A1 Littlejohn, RO
A1 Pfundt, R
A1 Mercimek-Andrews, S
A1 Stegmann, APA
A1 Kant, SG
A1 McLean, S
A1 Joss, S
A1 Swagemakers, SMA
A1 Douzgou, S
A1 Wall, SA
A1 Küry, S
A1 Calpena, E
A1 Koelling, N
A1 McGowan, SJ
A1 Twigg, SRF
A1 Mathijssen, IMJ
A1 Nellaker, C
A1 Brunner, HG
A1 Wilkie, AOM
PB Elsevier
YR 2018
JF https://openaccess.sgul.ac.uk/id/eprint/109920/1/1-s2.0-S0002929718301617-main.pdf
LK http://dx.doi.org/https://openaccess.sgul.ac.uk/id/eprint/109920/
DO https://openaccess.sgul.ac.uk/id/eprint/109920/
SF ELIB - SuUB Bremen

Export

RefWorks (nur Desktop-Version!)
Flow (Zuerst in Flow einloggen, dann importieren)