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PMID: 3239571 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13.

American journal of medical genetics ·Vol. 31 ·No. 4 ·1988-12-00 ·Pages 799-804

Brueton L, Huson SM, Winter RM, Williamson R

Abstract

Greig cephalopolysyndactyly syndrome (GCPS) is a rare autosomal dominant form of complex polydactyly. GCPS has been tentatively assigned to chromosome 7 on the basis of association of the condition with balanced translocations involving the short arm of chromosome 7 (7p13) in two families. Seven GCPS pedigrees with no chromosome abnormality were studied, and linkage was demonstrated between GCPS and the DNA sequence coding for the receptor for epidermal growth factor (localised to 7p12-13) (Z = 3.17; O = theta).

MeSH Terms
Chromosomes, Human, Pair 7 DNA Probes Foot Deformities/genetics Hand Deformities/genetics Humans Pedigree
Chemicals
DNA Probes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Brueton L
Division of Inherited Metabolic Disease, Northwick Park Hospital, Harrow, Middlesex, United Kingdom.
Huson S M
Winter R M
Williamson R
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1988-12-00
Pages
799-804
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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