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1 Ergebnisse
1
Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–B..:
de Stefano, Maria Chiara
;
Gallagher, Louise
;
Rakic, Severin
...
https://www.mdpi.com/1660-4601/17/24/9253. , 2020
Link:
http://hdl.handle.net/10400.16/2648
RT Journal T1
Rare Pathogenic Copy Number Variation in the 16p11.2 (BP4–BP5) Region Associated with Neurodevelopmental and Neuropsychiatric Disorders: A Review of the Literature
UL https://suche.suub.uni-bremen.de/peid=base-ftchporto:oai:repositorio.chporto.pt:10400.16_2648&Exemplar=1&LAN=DE A1 de Stefano, Maria Chiara A1 Gallagher, Louise A1 Rakic, Severin A1 Jorge, Paula A1 Cuturilo, Goran A1 Markovska-Simoska, Silvana A1 Borg, Isabella A1 Wolstencroft, Jeanne A1 Tümer, Zeynep A1 Harwood, Adrian J A1 Kodra, Yllka A1 Skuse, David PB MDPI YR 2020 K1 16p11.2 deletion K1 16p11.2 duplication K1 BP4–BP5 K1 copy numbers variants K1 neurodevelopmental disorders K1 rare diseases JF https://www.mdpi.com/1660-4601/17/24/9253 LK http://hdl.handle.net/10400.16/2648 DO http://hdl.handle.net/10400.16/2648 SF ELIB - SuUB Bremen
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