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Bachmann-Gagescu, R., Mefford, H.C., Cowan, C., Glew, G.M., Hing, A.V., Wallace, S., Bader, P.I., Hamati, A., Reitnauer, P.J., Smith, R., Stockton, D.W., Muhle, H., Helbig, I., Eichler, E.E., Ballif, B.C., Rosenfeld, J. and Tsuchiya, K.D. (2010) Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Genetic Medicine, 12, 641-647. http://dx.doi.org/10.1097/GIM.0b013e3181ef4286

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