1 Publication
2010
Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.
Bachmann Gagescu, RuxandraMefford, HeatherCowan, CharlesGlew, Gwen MHing, AnneWallace, StephanieBader, Patricia IHamati, Aline IReitnauer, Pamela JSmith, RosemarieStockton, David WMuhle, HiltrudHelbig, IngoEichler, EvanBallif, Blake CRosenfeld, Jill and Tsuchiya, Karen D
Genetics in medicine : official journal of the American College of Medical Genetics, vol. 12, (no. 10), pp. 641-7, 2010/Oct. | Journal Article