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1 Ergebnisse
1
Clinical Utility of a Unique Genome-Wide DNA Methylation Si..:
Foroutan A
;
Haghshenas S
;
Bhai P
...
info:eu-repo/semantics/altIdentifier/pmid/35163737. , 2022
Link:
http://hdl.handle.net/10447/547094
RT Journal T1
Clinical Utility of a Unique Genome-Wide DNA Methylation Signature for KMT2A-Related Syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftunivpalermo:oai:iris.unipa.it:10447_547094&Exemplar=1&LAN=DE A1 Foroutan A A1 Haghshenas S A1 Bhai P A1 Levy M. A A1 Kerkhof J A1 McConkey H A1 Niceta M A1 Ciolfi A A1 Pedace L A1 Miele E A1 Genevieve D A1 Heide S A1 Alders M A1 Zampino G A1 Merla G A1 Fradin M A1 Bieth E A1 Bonneau D A1 Dieterich K A1 Fergelot P A1 Schaefer E A1 Faivre L A1 Vitobello A A1 Maitz S A1 Fischetto R A1 Gervasini C A1 Piccione M A1 van de Laar I A1 Tartaglia M A1 Sadikovic B A1 Lebre A. -S PB MDPI; country:CH YR 2022 K1 Abnormalities K1 Multiple K1 Craniofacial Abnormalitie K1 DNA methylation K1 Epigenetic K1 Episignature K1 Facie K1 Growth Disorder K1 Human K1 Hypertrichosi K1 Intellectual disability K1 KMT2A gene K1 Neurodevelopmental disorder K1 Phenotype K1 Wiedemann–Steiner syndrome JF info:eu-repo/semantics/altIdentifier/pmid/35163737 LK http://hdl.handle.net/10447/547094 DO http://hdl.handle.net/10447/547094 SF ELIB - SuUB Bremen
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