Greig cephalopolysyndactyly syndrome: A possible mouse homologue (Xt‐extra toes)
- 1 December 1988
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 31 (4) , 793-798
- https://doi.org/10.1002/ajmg.1320310411
Abstract
Greig cephalopolysyndactyly syndrome is an autosomal dominant form of complex polydactyly in man. Attention is called to the evidence that, on both morphological and comparative gene mapping grounds, this defect is homologous to Xt‐extra toes in the mouse. The pattern of polydactyly in both species is very similar. In addition, both conditions probably map close to the T‐cell receptor gamma polypeptide at 13 A2–3 in mouse and 7p15 in humans.Keywords
This publication has 17 references indexed in Scilit:
- Malformation syndromes: a review of mouse/human homology.Journal of Medical Genetics, 1988
- Chromosome maps of man and mouse, IIIGenomics, 1987
- The Greig cephalopolysyndactyly syndrome: Report of a family and review of the literatureAmerican Journal of Medical Genetics, 1985
- A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly‐craniofacial anomalies syndromeAmerican Journal of Medical Genetics, 1983
- Frontonasal dysplasia, coronal cranisoynostosis, pre‐ and postaxial polydactyly and split nails: a new autosomal dominant mutant with reduced penetrance and varibale expression?Clinical Genetics, 1983
- The greig cephalopolysyndactyly syndrome in a canadian familyAmerican Journal of Medical Genetics, 1982
- A NEWBORN INFANT WITH CRANIOFACIAL DYSMORPHISM AND POLYSYNDACTYLY (GREIG'S SYNDROME)Acta Paediatrica, 1981
- 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