Citations for
17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction.
Grisart B, Willatt L, Destrée A, Fryns JP, Rack K, de Ravel T, Rosenfeld J, Vermeesch JR, Verellen-Dumoulin C, Sandford R.
J Med Genet 46(8):524-30. Epub 2009 Jun 4. 2009
2DEL15Q13, DEL15Q24, DEL16P12, DEL17Q21, DEL1Q41, DEL2P15, DEL9Q22, DUP17Q21
Novel microdeletion syndromes detected by chromosome microarrays.
Slavotinek AM.
Hum Genet May 30. [Epub ahead of print] 2008
A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features.
Kirchhoff M, Bisgaard AM, Duno M, Hansen FJ, Schwartz M.
Eur J Med Genet 50: 256-263 2007