Delineation of the clinical phenotype caused by de novo CLTC variants
Sa MJN, Venselaar H, Wiel L, Trimouille A, Lasseaux E, Naudion S, Lacombe D, Piton A, Vincent-Delorme C, Zweier C, Wiesmann da Silva Reis A, Trollmann R, Ruiz A, Gabau E, Vetro A, Guerrini R, Bakhtiari S, Kruer M, Crompton K, Amor DJ, Bijlsma EK, Barakat TS, Van Dooren MF, Pfundt R, Gilissen C, De Vries BB, De Brouwer AP, Koolen DA (2019)
Publication Type: Conference contribution
Publication year: 2019
Journal
Publisher: NATURE PUBLISHING GROUP
City/Town: LONDON
Pages Range: 1381-1381
Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS
Event location: Gothenburg, SWEDEN
Authors with CRIS profile
Christiane Zweier
Medizinische Fakultät
André Wiesmann da Silva Reis
Lehrstuhl für Humangenetik
Regina Trollmann
Professur für Kinder- u. Jugendmedizin Schwerpunkt Neuropädiatrie
Involved external institutions
Autonomous University of Barcelona (UAB) / Universitat Autònoma de Barcelona
Spain (ES)
Erasmus University Medical Center (MC)
Netherlands (NL)
University of Arizona
United States (USA) (US)
Radboud University Nijmegen Medical Centre / Radboudumc of voluit Radboud Universitair Medisch Centrum (UMC)
Netherlands (NL)
Hôpital Jeanne de Flandre
France (FR)
Centre Hospitalier Universitaire de Bordeaux / CHU Bordeaux
France (FR)
Università degli Studi di Firenze / University of Florence
Italy (IT)
Royal Children's Hospital Parkville
Australia (AU)
National Institute for Health and Medical Research / Institut national de la santé et de la recherche médicale (INSERM)
France (FR)
Leiden University
Netherlands (NL)
Spain (ES)
Erasmus University Medical Center (MC)
Netherlands (NL)
University of Arizona
United States (USA) (US)
Radboud University Nijmegen Medical Centre / Radboudumc of voluit Radboud Universitair Medisch Centrum (UMC)
Netherlands (NL)
Hôpital Jeanne de Flandre
France (FR)
Centre Hospitalier Universitaire de Bordeaux / CHU Bordeaux
France (FR)
Università degli Studi di Firenze / University of Florence
Italy (IT)
Royal Children's Hospital Parkville
Australia (AU)
National Institute for Health and Medical Research / Institut national de la santé et de la recherche médicale (INSERM)
France (FR)
Leiden University
Netherlands (NL)
How to cite
APA:
Sa, M.J.N., Venselaar, H., Wiel, L., Trimouille, A., Lasseaux, E., Naudion, S.,... Koolen, D.A. (2019). Delineation of the clinical phenotype caused by de novo CLTC variants. In EUROPEAN JOURNAL OF HUMAN GENETICS (pp. 1381-1381). Gothenburg, SWEDEN: LONDON: NATURE PUBLISHING GROUP.
MLA:
Sa, M. J. Nabais, et al. "Delineation of the clinical phenotype caused by de novo CLTC variants." Proceedings of the 52nd Conference of the European-Society-of-Human-Genetics (ESHG), Gothenburg, SWEDEN LONDON: NATURE PUBLISHING GROUP, 2019. 1381-1381.
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