Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23.
David Mowat(UNSW Sydney), Meredith Wilson(Children's Hospital at Westmead), Geoffrey David Hain Croaker(Alexandra Hospital), Bronwyn Kerr(Manchester Academic Health Science Centre), Daniel T. Cass(St Michael’s Hospital), Lesley C. Adès(The University of Sydney), Jeffrey Chaitow(Alexandra Hospital), Nicole Chia(Alexandra Hospital)
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