TY  - JOUR
T1  - GReig cephalopolysyndactyly syndrome
AU  - Duncan PA, Klein RM, Wilmot PL, Shapiro LR
Y1  - 1979/08/01
N1  - 10.1001/archpedi.1979.02130080058010
JO  - American Journal of Diseases of Children
SP  - 818
EP  - 821
VL  - 133
IS  - 8
N2  - • Based on the family presented and five others previously described, it can be concluded that the Grieg cephalopolysyndactyly syndrome is a fully penetrant autosomal dominant disease consisting of four variably expressed malformations: postaxial polydactyly (type B), preaxial polydactyly, syndactyly, and minor craniofacial abnormalities. This entity can be differentiated from other craniofacial-digital syndromes because of the absence of mental retardation, craniosynostosis, and brachydactyly.(Am J Dis Child 133:818-821, 1979)
SN  - 0002-922X
M3  - doi: 10.1001/archpedi.1979.02130080058010
UR  - http://dx.doi.org/10.1001/archpedi.1979.02130080058010
ER  -