Erich Roessler, Yong Ma, Maia Ouspenskaia, Felicitas Lacbawan, Claude Bendavid, et al.. Truncating loss-of-function mutations of DISP1 contribute to holoprosencephaly-like microform features in humans..
Human Genetics, Springer Verlag, 2009, 125 (4), pp.393-400.
⟨10.1007/s00439-009-0628-7⟩.
⟨inserm-00366120⟩