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1 Ergebnisse
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De novo and inherited pathogenic variants in KDM3B cause in..:
Diets, I.J
;
van der Donk, R
;
Baltrunaite, K
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.02.023. , 2019
Link:
https://push-zb.helmholtz-muenchen.de/frontdoor.php?so..
RT Journal T1
De novo and inherited pathogenic variants in KDM3B cause intellectual disability, short stature, and facial dysmorphism
UL https://suche.suub.uni-bremen.de/peid=base-fthzmuenchen:oai:opus-zb.helmholtz-muenchen.de:55790&Exemplar=1&LAN=DE A1 Diets, I.J A1 van der Donk, R A1 Baltrunaite, K A1 Waanders, E A1 Reijnders, M.R.F A1 Dingemans, A.J.M A1 Pfundt, R A1 Vulto-van Silfhout, A.T A1 Wiel, L A1 Gilissen, C A1 Thevenon, J A1 Perrin, L A1 Afenjar, A A1 Nava, C A1 Keren, B A1 Bartz, S A1 Peri, B A1 Beunders, G A1 Verbeek, N A1 van Gassen, K A1 Thiffault, I A1 Cadieux-Dion, M A1 Huerta-Saenz, L A1 Wagner, M A1 Konstantopoulou, V A1 Vodopiutz, J A1 Griese, M A1 Boel, A A1 Callewaert, B A1 Brunner, H.G A1 Kleefstra, T A1 Hoogerbrugge, N A1 de Vries, B.B.A A1 Hwa, V A1 Dauber, A A1 Hehir-Kwa, J.Y A1 Kuiper, R.P A1 Jongmans, M.C.J PB Cell Press YR 2019 K1 Kdm3b K1 Cancer Predisposition K1 Developmental Delay K1 Facial Recognition K1 Intellectual Disability K1 Leukemia K1 Lymphoma K1 Short Stature JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2019.02.023 LK http://dx.doi.org/https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=55790 DO https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=55790 SF ELIB - SuUB Bremen
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