Citations for

1	HPEL1, TDGF1
	A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
	De La Cruz JM, Bamford RN, Burdine RD, Roessler E, Barkovich AJ, Donnai D, Schier AF, Muenke M.
	Hum Genet 110(5):422-8. 2002