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CTCF variants in 39 individuals with a variable neurodevelo..:

Konrad, Enrico D.H ; Nardini, Niels ; Caliebe, Almuth...
Konrad , E D H , Nardini , N , Caliebe , A , Nagel , I , Young , D , Horvath , G , Santoro , S L , Shuss , C , Ziegler , A , Bonneau , D , Kempers , M , Pfundt , R , Legius , E , Bouman , A , Stuurman , K E , Õunap , K , Pajusalu , S , Wojcik , M H , Vasileiou , G , Le Guyader , G , Schnelle , H M , Berland , S , Zonneveld-Huijssoon , E , Kersten , S , Gupta , A , Blackburn , P R , Ellingson , M S , Ferber , M J , Dhamija , R , Klee , E W , McEntagart , M , Lichtenbelt , K D , Kenney , A , Vergano , S A , Abou Jamra , R , Platzer , K , Ella Pierpont , M , Khattar , D , Hopkin , R J , Martin , R J , Jongmans , M C J , Chang , V Y , Martinez-Agosto , J A , Kuismin , O , Kurki , M I , Pietiläinen , O , Palotie , A , Maarup , T J , Venborg Pedersen , K , Laulund , L W & DDD Study 2019 , ' CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum ' , Genetics in Medicine , vol. 21 , no. 12 , pp. 2723-2.... , 2019

Link: https://portal.findresearcher.sdu.dk/da/publications/1..

RT Journal
T1 <Title>CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsydanskunivpub:oai:sdu.dk:publications_1124fece-8bda-40ef-8f71-3f14a754f01f&Exemplar=1&LAN=DE
				
A1 Konrad, Enrico D.H
A1 Nardini, Niels
A1 Caliebe, Almuth
A1 Nagel, Inga
A1 Young, Dana
A1 Horvath, Gabriella
A1 Santoro, Stephanie L
A1 Shuss, Christine
A1 Ziegler, Alban
A1 Bonneau, Dominique
A1 Kempers, Marlies
A1 Pfundt, Rolph
A1 Legius, Eric
A1 Bouman, Arjan
A1 Stuurman, Kyra E
A1 Õunap, Katrin
A1 Pajusalu, Sander
A1 Wojcik, Monica H
A1 Vasileiou, Georgia
A1 Le Guyader, Gwenaël
A1 Schnelle, Hege M
A1 Berland, Siren
A1 Zonneveld-Huijssoon, Evelien
A1 Kersten, Simone
A1 Gupta, Aditi
A1 Blackburn, Patrick R
A1 Ellingson, Marissa S
A1 Ferber, Matthew J
A1 Dhamija, Radhika
A1 Klee, Eric W
A1 McEntagart, Meriel
A1 Lichtenbelt, Klaske D
A1 Kenney, Amy
A1 Vergano, Samantha A
A1 Abou Jamra, Rami
A1 Platzer, Konrad
A1 Ella Pierpont, Mary
A1 Khattar, Divya
A1 Hopkin, Robert J
A1 Martin, Richard J
A1 Jongmans, Marjolijn C.J
A1 Chang, Vivian Y
A1 Martinez-Agosto, Julian A
A1 Kuismin, Outi
A1 Kurki, Mitja I
A1 Pietiläinen, Olli
A1 Palotie, Aarno
A1 Maarup, Timothy J
A1 Venborg Pedersen, Katja
A1 Laulund, Lone W
YR 2019
K1 chromatin organization
K1 CTCF
K1 Drosophila melanogaster
K1 intellectual disability
K1 neurodevelopmental disorders
JF Konrad , E D H , Nardini , N , Caliebe , A , Nagel , I , Young , D , Horvath , G , Santoro , S L , Shuss , C , Ziegler , A , Bonneau , D , Kempers , M , Pfundt , R , Legius , E , Bouman , A , Stuurman , K E , Õunap , K , Pajusalu , S , Wojcik , M H , Vasileiou , G , Le Guyader , G , Schnelle , H M , Berland , S , Zonneveld-Huijssoon , E , Kersten , S , Gupta , A , Blackburn , P R , Ellingson , M S , Ferber , M J , Dhamija , R , Klee , E W , McEntagart , M , Lichtenbelt , K D , Kenney , A , Vergano , S A , Abou Jamra , R , Platzer , K , Ella Pierpont , M , Khattar , D , Hopkin , R J , Martin , R J , Jongmans , M C J , Chang , V Y , Martinez-Agosto , J A , Kuismin , O , Kurki , M I , Pietiläinen , O , Palotie , A , Maarup , T J , Venborg Pedersen , K , Laulund , L W & DDD Study 2019 , ' CTCF variants in 39 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum ' , Genetics in Medicine , vol. 21 , no. 12 , pp. 2723-2...
LK http://dx.doi.org/https://portal.findresearcher.sdu.dk/da/publications/1124fece-8bda-40ef-8f71-3f14a754f01f
DO https://portal.findresearcher.sdu.dk/da/publications/1124fece-8bda-40ef-8f71-3f14a754f01f
SF ELIB - SuUB Bremen

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