المؤلفون: Duncan, A.R. (Anna R.), Vitobello, A. (Antonio), Collins, S.C. (Stephan C.), Vancollie, V.E. (Valerie E.), Lelliott, C.J. (Christopher J.), Rodan, L. (Lance), Shi, J. (Jiahai), Seman, A.R. (Ann R.), Agolini, E. (Emanuele), Novelli, A. (Antonio), Prontera, P. (Paolo), Guillen Sacoto, M.J. (Maria J.), Santiago-Sim, T. (Teresa), Trimouille, A. (Aurélien), Goizet, C. (Cyril), Nizon, M. (Mathilde), Bruel, A.-L. (Ange-Line), Philippe, C. (Christophe), Grant, P.E. (Patricia E.), Wojcik, M.H. (Monica H.), Stoler, J. (Joan), Genetti, C.A. (Casie A.), Dooren, M.F. (Marieke) van, Maas, S.M. (Saskia), Alders, M. (Mariëlle), Faivre, L. (Laurence), Sorlin, A. (Arthur), Yoon, G. (Grace), Yalcin, B. (Binnaz), Agrawal, P.B. (Pankaj B.)

المصدر: American Journal of Human Genetics vol. 107 no. 6, pp. 1170-1177

مصطلحات موضوعية: agenesis of the corpus callosum, dysmorphic hippocampi, global developmental delay, heterozygous variant, intellectual disability, JMJD2B, KDM4B, neurodevelopmental disorder

وصف الملف: application/pdf

Relation: https://repub.eur.nl/pub/132482; urn:hdl:1765/132482

الاتاحة: https://repub.eur.nl/pub/132482
https://doi.org/10.1016/j.ajhg.2020.11.001