| Literature DB >> 8761882 |
R A Clarke1, J H Kearsley, D A Walsh.
Abstract
Klippel-Feil syndrome (KFS) is characterised by congenital fusion of vertebrae within the rostral spine. The first KFS gene (SGM1) locus identified on chromosome 8 segregates with vertebral fusions and associated vocal impairment within the KF2-01 family (Clarke et al., '94, '95). Here, we describe the unique pattern of variable phenotypic expression within the KF2-01 family. The pattern of anomalies revealed a cumulative, rostrocaudal graded sequence of skipped vertebral fusions. This fusion pattern presents striking similarities with the mutant phenotype and gene expression profile of the Drosophila segment polarity gene engrailed.Entities:
Mesh:
Year: 1996 PMID: 8761882 DOI: 10.1002/(SICI)1096-9926(199603)53:3<152::AID-TERA2>3.0.CO;2-6
Source DB: PubMed Journal: Teratology ISSN: 0040-3709