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Literature for DOID 0110873: holoprosencephaly 9
Xenbase Articles
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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.,
Roessler E,Du YZ,Mullor JL,Casas E,Allen WP,Gillessen-Kaesbach G,Roeder ER,Ming JE,Ruiz i Altaba A,Muenke M,
Proc Natl Acad Sci U S A. November 11, 2003; 100(23):1091-6490.
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