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
Publisher: NATURE PUBLISHING GROUP
City/Town: LONDON
Pages Range: 1116-1117
Conference Proceedings Title: EUROPEAN JOURNAL OF HUMAN GENETICS
DOI: 10.1038/s41436-019-0585-z
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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