A complex bilateral polysyndactyly disease locus maps to chromosome 7q36
- 1 March 1994
- journal article
- research article
- Published by Springer Nature in Nature Genetics
- Vol. 6 (3) , 282-286
- https://doi.org/10.1038/ng0394-282
Abstract
We demonstrate that the gene responsible for a congenital limb deformity (polysyndactyly) maps to chromosome 7q36 in a large family. Pre– and postaxial anomalies of the extremities are inherited in this family as an autosomal dominant trait. The disease locus is closely linked to D7S550 (maximum lod score = 6.85, θ = 0). This region is homologous to a segment of mouse chromosome 5, where the mutations hammer toe (HM) and hemimelic extra toes (HX) have been mapped. These data suggest that human chromosome 7q36 and the homologous region of mouse chromosome 5 contain genes involved in limb pattern formation.Keywords
This publication has 16 references indexed in Scilit:
- Closure of a genetic linkage map of human chromosome 7q with centromere and telomere polymorphismsGenomics, 1992
- A Comprehensive Genetic Linkage Map of the Human GenomeScience, 1992
- A second-generation linkage map of the human genomeNature, 1992
- GLI3 zinc-finger gene interrupted by translocations in Greig syndrome familiesNature, 1991
- Mapping of the two mouse engrailed-like genes: Close linkage of En-1 to dominant hemimelia (Dh) on chromosome 1 and of En-2 to hemimelic extra-toes (Hx) on chromosome 5Genomics, 1990
- Isolation and chromosomal localization of the human En-2 geneGenomics, 1989
- A family with complex bilateral polysyndactyThe Journal of Hand Surgery, 1988
- Female external genitalia and müllerian duct derivatives in a 46,XY infant with the Smith‐Lemli‐Opitz syndromeAmerican Journal of Medical Genetics, 1987
- Polydactyly in the BibleThe Journal of Hand Surgery, 1986
- The Study of Genetic Variation in NigeriaHuman Heredity, 1976