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E. Jabs, Cathleen Coss, S. Hayflick, Theodore Whitmore, Richard Pauli, Richard Pauli, Susan Kirkpatrick, Deborah Meyers, Rosalie Goldberg, Donald Day, Kenneth Rosenbaum (1991)
Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this region.Genomics, 11 1
A Franceschetti (1944)
Un syndrome nouveau; la dysostose mandibulo‐faciale, 1
J. Weissenbach, G. Gyapay, C. Dib, A. Vignal, J. Morissette, P. Millasseau, G. Vaysseix, M. Lathrop (1992)
A second-generation linkage map of the human genomeNature, 359
E Treacher Collins (1900)
Cases with symmetrical congenital notches in the outer part of each lid and defective development of the malar bones, 20
Michael Dixon, Andrew Read, Dian Donnai, Alison Colley, Joanne Dixon, R. Williamson (1991)
The gene for Treacher Collins syndrome maps to the long arm of chromosome 5.American journal of human genetics, 49 1
A Franceschetti, D Klein (1949)
Mandibulo‐facial dysostosis: New hereditry syndrome, 27
Michael Dixon, Jill Dixon, T. Houseal, M. Bhatt, David Ward, Katherine Klinger, Gregory Landes (1993)
Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.American journal of human genetics, 52 5
E. Jabs, Xiang Li, Cathleen Coss, Eugene Taylor, Deborah Meyers, James Weber (1991)
Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.Genomics, 11 1
M. Wiley, P. Cauwenbergs, I. Taylor (1983)
Effects of retinoic acid on the development of the facial skeleton in hamsters: early changes involving cranial neural crest cells.Acta anatomica, 116 2
Susan Herring, Ursula Rowlatt, Samuel Pruzansky, J. Optiz (1979)
Anatomical abnormalities in mandibulofacial dysostosis.American journal of medical genetics, 3 3
Sulik Kk, Malcolm Johnston, Smiley Sj, Speight Hs, Jarvis Be (1987)
Mandibulofacial dysostosis (Treacher Collins syndrome): a new proposal for its pathogenesis.American journal of medical genetics, 27 2
K. Jones, David Smith, M. Harvey, B. Hall, L. Quan (1975)
Older paternal age and fresh gene mutation: data on additional disorders.The Journal of pediatrics, 86 1
D. Poswillo (1975)
The pathogenesis of the treacher Collins syndrome (Mandibulofacial dysostosis)British Journal of Oral Surgery, 13
RJ Gorlin, MM Cohen, LS Levin (1990)
Syndromes of the Head and Neck
A Vignal, G Gyapay, J Hazan, S Nguyen, C Dupraz, N Cheron, N Becuwe, M Tranchant (1993)
Methods in Molecular Genetics: Gene and Chromosome Analysis, 1
M. Dixon, J. Dixon, D. Rašková, M. Beau, R. Williamson, K. Klinger, G. Landes (1992)
Genetic and physical mapping of the Treacher Collins syndrome locus: refinement of the localization to chromosome 5q32-33.2.Human molecular genetics, 1 4
E. Jabs, X. Li, M. Lovett, L. Yamaoka, E. Taylor, M. Speer, C. Coss, R. Cadle, B. Hall, K. Brown (1993)
Genetic and physical mapping of the Treacher Collins syndrome locus with respect to loci in the chromosome 5q3 region.Genomics, 18 1
G. Lathrop, J. Lalouel, C. Julier, J. Ott (1985)
Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.American journal of human genetics, 37 3
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 θ = 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 analysis [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. © 1994 Wiley‐Liss, Inc.
American Journal of Medical Genetics Part A – Wiley
Published: Mar 15, 1995
Keywords: ; ; ; ;
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