Phenotypic and functional consequences of haploinsufficiency of genes from exocyst and retinoic acid pathway due to a recurrent microdeletion of 2p13.2

J. Wen, F. Lopes, G. Soares, S.A. Farrell, C. Nelson, Y. Qiao, S. Martell, C. Badukke, C. Bessa, B. Ylstra, S. Lewis, N. Isoherranen, P. Maciel, E. Rajcan-Separovic

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Article number100
JournalOrphanet Journal of Rare Diseases
Publication statusPublished - 2013

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