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1 Ergebnisse
1
De Novo and Inherited Loss-of-Function Variants in TLK2: Cl..:
Reijnders, MRF
;
Miller, KA
;
Alvi, M
...
issn:0002-9297. , 2018
Link:
http://hdl.handle.net/11343/255206
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-ftumelbourne:oai:jupiter.its.unimelb.edu.au:11343_255206&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 BV YR 2018 JF issn:0002-9297 LK http://hdl.handle.net/11343/255206 DO http://hdl.handle.net/11343/255206 SF ELIB - SuUB Bremen
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