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PMID: 7802004 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Apparent genetic homogeneity of the Treacher Collins-Franceschetti syndrome.

American journal of medical genetics ·Vol. 52 ·No. 2 ·1994-08-15 ·Pages 174-7

Edery P, Manach Y, Le Merrer M, Till M, Vignal A, Lyonnet S, Munnich A

Abstract

The Treacher Collins-Franceschetti syndrome (TCOF) or mandibulofacial dysostosis (MFD) is an autosomal dominant disorder characterized by craniofacial abnormalities and hearing loss. A refined genetic linkage map of the TCOF locus was established in 8 independent families, using 12 microsatellite DNA markers of the distal 5q. Positive lod score values were obtained for all markers with a maximum at the D5S413 locus (Zmax = 3.79 at theta = 0%). Multipoint linkage analysis and haplotype analysis supported the location of the gene between loci D5S434 and D5S412. These results are consistent with previous linkage analyses [Dixon et al.: Am J Hum Genet 49:17-22, 1991, Am J Hum Genet 52:907-914, 1993; Jabs et al.: Genomics 11:193-198, 1991, Genomics 18:7-13, 1993] and provide further evidence of genetic homogeneity in this syndrome.

MeSH Terms
Chromosomes, Human, Pair 5 DNA, Satellite/genetics Female Genes, Dominant Genotype Haplotypes/genetics Humans Lod Score Male Mandibulofacial Dysostosis/genetics Pedigree Repetitive Sequences, Nucleic Acid
Chemicals
DNA, Satellite
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Edery P
Unité de Recherches sur les Handicaps Génétiques de l'Enfant INSERM U-393, Hôpital des Enfants Malades, Paris, France.
Manach Y
Le Merrer M
Till M
Vignal A
Lyonnet S
Munnich A
Article Info
Journal
American journal of medical genetics
Abbr.
Am J Med Genet
ISSN
0148-7299
Published
1994-08-15
Pages
174-7
Language
English
Region
United States
NLM ID
7708900
Subset
IM
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