Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7356
Citations
Scopus Web of ScienceĀ® Altmetric
?
?
Type: Journal article
Title: Localization of craniosynostosis Adelaide type to 4p16
Author: Hollway, G.
Phillips, H.
Ades, L.
Haan, E.
Muley, J.
Citation: Human Molecular Genetics, 1995; 4(4):681-683
Publisher: IRL Press
Issue Date: 1995
ISSN: 0964-6906
1460-2083
Abstract: Craniosynostosis Adelaide type is a rare autosomal dominant syndrome associated with digital abnormalities. Linkage mapping was carried out excluding allelism to Saethre-Chotzen syndrome at 7p21, craniosynostosis Boston type at 5q34-q35, Jackson-Weiss and Crouzon syndromes at 10q24-q25 and Pfeiffer syndrome mapping near 8cen. Exclusion mapping was extended to the entire genome until linkage to chromosome 4 was detected. A maximum two-point lod score of 6.2 (theta = 0.0) was obtained with D4S412. The gene responsible for craniosynostosis Adelaide type was localized to 4p16, telomeric to D4S394. This region contains two plausible candidate genes, the MSX1 (HOX7) homeobox gene and the FGFR3 fibroblast growth factor receptor gene.
Keywords: Chromosomes, Human, Pair 4; Humans; Craniosynostoses; Homeodomain Proteins; Receptors, Fibroblast Growth Factor; Transcription Factors; Chromosome Mapping; Genes, Dominant; Phenotype; MSX1 Transcription Factor
RMID: 0030005599
DOI: 10.1093/hmg/4.4.681
Appears in Collections:Paediatrics publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.