| 1 | DUP17Q21
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| 17q21.31 microduplication patients are characterised by behavioural problems and poor social interaction.
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| Grisart B, Willatt L, Destrée A, Fryns JP, Rack K, de Ravel T, Rosenfeld J, Vermeesch JR, Verellen-Dumoulin C, Sandford R.
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| J Med Genet 46(8):524-30. Epub 2009 Jun 4.
2009
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| 2 | DEL15Q13, DEL15Q24, DEL16P12, DEL17Q21, DEL1Q41, DEL2P15, DEL9Q22, DUP17Q21
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| Novel microdeletion syndromes detected by chromosome microarrays.
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| Slavotinek AM.
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| Hum Genet May 30. [Epub ahead of print] 2008
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| 3 | CRHR1,DUP17Q21,MAPT
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| A 17q21.31 microduplication, reciprocal to the newly described 17q21.31 microdeletion, in a girl with severe psychomotor developmental delay and dysmorphic craniofacial features.
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| Kirchhoff M, Bisgaard AM, Duno M, Hansen FJ, Schwartz M.
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| Eur J Med Genet 50: 256-263 2007
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