CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum

Konrad E, Nardini N, Blyth M, Prescott K, Bouman AM, Brilstra EH, Caliebe A, Ibitoye R, Chang VY, Gupta A, Le Guyader G, Jamra RA, Platzer K, Jongmans MCJ, Kenney A, Kempers M, Pfundt R, Khattar D, Kuismin O, Legius E, Lichtenbelt KD, Maarup TJ, Mcentagart M, Ounap K, Pierpont ME, Santoro SL, Schnelle HM, Fassi E, Young D, Ziegler A, Gregor A, Van Esch H, Zweier C (2019)

Publication Type: Conference contribution

Publication year: 2019

Journal

Publisher: NATURE PUBLISHING GROUP

City/Town: LONDON

Pages Range: 1116-1117

Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS

Event location: Gothenburg

DOI: 10.1038/s41436-019-0585-z

Authors with CRIS profile

Additional Organisation(s)

Involved external institutions

Universität Leipzig Germany (DE) Leeds Teaching Hospitals NHS Trust United Kingdom (GB) Katholieke Universiteit Leuven (KUL) / Catholic University of Leuven Belgium (BE) Kaiser Permanente United States (USA) (US) University of California Los Angeles (UCLA) United States (USA) (US) St George's, University of London (SGUL) / St George's Hospital Medical School United Kingdom (GB) Mayo Clinic United States (USA) (US) Cincinnati Children's Hospital Medical Center United States (USA) (US) University of British Columbia Canada (CA) Radboud University Nijmegen Netherlands (NL) Oulu University Hospital Finland (FI) Washington University United States (USA) (US) Erasmus University Medical Center (MC) Netherlands (NL) Centre hospitalier universitaire de Poitiers (CHU de Poitiers) France (FR) Children's Hospital of The King's Daughters United Kingdom (GB) Tartu University Hospital Estonia (EE) University Medical Centre Utrecht (UMC Utrecht) Netherlands (NL) University of Minnesota (UMN) United States (USA) (US) Universiteit Utrecht (UU) / Utrecht University Netherlands (NL) Ohio State University United States (USA) (US) The Griffin Institute - Northwick Park Institute for Medical Research (NPIMR) United Kingdom (GB) Haukeland University Hospital / Haukeland universitetssykehus Norway (NO) Universitätsklinikum Schleswig-Holstein (UKSH) Germany (DE) Centre hospitalier universitaire (CHU) d'Angers France (FR)

How to cite

APA:

Konrad, E., Nardini, N., Blyth, M., Prescott, K., Bouman, A.M., Brilstra, E.H.,... Zweier, C. (2019). CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 1116-1117). Gothenburg, SE: LONDON: NATURE PUBLISHING GROUP.

MLA:

Konrad, Enrico, et al. "CTCF variants in 31 individuals with a variable neurodevelopmental disorder broaden the mutational and clinical spectrum." Proceedings of the 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg LONDON: NATURE PUBLISHING GROUP, 2019. 1116-1117.

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