Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F D Hannes, A J Sharp, H C Mefford, T de Ravel, C A Ruivenkamp, M H Breuning, J-P Fryns, K Devriendt, G Van Buggenhout, A Vogels, H Stewart, R C Hennekam, G M Cooper, R Regan, S J L Knight, E E Eichler, and J R Vermeesch
J Med Genet 2009 46: 223-232.
F D Hannes, A J Sharp, H C Mefford, T de Ravel, C A Ruivenkamp, M H Breuning, J-P Fryns, K Devriendt, G Van Buggenhout, A Vogels, H Stewart, R C Hennekam, G M Cooper, R Regan, S J L Knight, E E Eichler, and J R Vermeesch
J Med Genet 2009 46: 223-232.
web only appendices 46/4/223
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