ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome

Chromosomal abnormalities are implicated in a substantial number of human developmental syndromes, but for many such disorders little is known about the causative genes. The recently described 1q41q42 microdeletion syndrome is characterized by characteristic dysmorphic features, intellectual disabil...

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Bibliographic Details
Main Authors:	Zak, J, Vives, V, Szumska, D, Vernet, A, Schneider, J, Miller, P, Slee, E, Joss, S, Lacassie, Y, Chen, E, Escobar, L, Tucker, M, Aylsworth, A, Dubbs, H, Collins, A, Andrieux, J, Dieux-Coeslier, A, Haberlandt, E, Kotzot, D, Scott, D, Parker, M, Zakaria, Z, Choy, Y, Wieczorek, D, Innes, A, Jun, K, Zinner, S, Prin, F, Lygate, C, Pretorius, P, Rosenfeld, J, Mohun, T, Lu, X
Format:	Journal article
Language:	English
Published:	Nature Publishing Group 2016

ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome

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