Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/7354
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Type: Journal article
Title: Molecular dissection of a contiguous gene syndrome: Localization of the genes involved in the Langer-Giedion syndrome
Author: Ludecke, H.
Wagner, M.
Nardmann, J.
La Pillo, B.
Parrish, J.
Willems, P.
Sutherland, G.
Citation: Human Molecular Genetics, 1995; 4(1):31-36
Publisher: IRL Press
Issue Date: 1995
ISSN: 0964-6906
1460-2083
Abstract: The Langer-Giedion syndrome (tricho-rhino-phalangeal syndrome type II, TRPS II) is characterized by craniofacial dysmorphism and skeletal abnormalities. It combines the clinical features of TRPS I and multiple cartilaginous exostoses (EXT). We have used YAC cloning, Southern blotting, PCR analysis, and fluorescence in situ hybridization to study chromosome 8 deletions, translocations, an inversion, and an insertion in patients with TRPS I, TRPS II or EXT. Our results indicate that the TRPS gene maps more than 1,000 kb proximal to the EXT1 gene and that both genes are affected in TRPS II. We conclude that TRPS II is not due to pleiotropic effects of mutations in a single gene, but that it is a true contiguous gene syndrome.
Keywords: Chromosomes, Artificial, Yeast; Chromosomes, Human, Pair 8; Humans; Langer-Giedion Syndrome; Translocation, Genetic; DNA Primers; In Situ Hybridization, Fluorescence; Chromosome Mapping; Mutagenesis, Insertional; Gene Deletion; Base Sequence; Molecular Sequence Data; Chromosome Inversion
RMID: 0030005601
DOI: 10.1093/hmg/4.1.31
Appears in Collections:Paediatrics publications

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