Greig cephalopolysyndactyly: report of 13 affected individuals in three families
- 30 September 1983
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 24 (4) , 257-265
- https://doi.org/10.1111/j.1399-0004.1983.tb00080.x
Abstract
Three families with Greig cephalopolysyndactyly are reported, the relationship with preaxial polydactyly type IV and acrocallosal syndrome is discussed.Keywords
This publication has 9 references indexed in Scilit:
- The greig cephalopolysyndactyly syndrome in a canadian familyAmerican Journal of Medical Genetics, 1982
- The acrocallosal syndromeAmerican Journal of Medical Genetics, 1982
- Acrocallosal syndromeAmerican Journal of Medical Genetics, 1982
- The Greig polysyndactyly craniofacial dysmorphism syndrome: Variable expression in a familyEuropean Journal of Pediatrics, 1981
- A NEWBORN INFANT WITH CRANIOFACIAL DYSMORPHISM AND POLYSYNDACTYLY (GREIG'S SYNDROME)Acta Paediatrica, 1981
- Hallux duplication, postaxial polydactyly, absence of the corpus callosum, severe mental retardation, and additional anomalies in two unrelated patients: A new syndromeAmerican Journal of Medical Genetics, 1980
- The Greig polysyndactyly-craniofacial dysmorphism syndromeEuropean Journal of Pediatrics, 1977
- Familial polysyndactyly and craniofacial anomaliesClinical Genetics, 1972
- Frontodigital syndrome: A dominantly inherited disorder with normal intelligenceThe Journal of Pediatrics, 1970