Literature DB >> 1765376

Mapping the Treacher Collins syndrome locus to 5q31.3----q33.3.

E W Jabs1, X Li, C A Coss, E W Taylor, D A Meyers, J L Weber.   

Abstract

Treacher Collins syndrome is an autosomal dominant disorder of abnormal craniofacial development. Linkage analysis was performed in Treacher Collins families with restriction fragment length or microsatellite polymorphisms associated with eight loci previously mapped to 5q31----qter. Positive lod scores were obtained for four loci, D5S119, D5S207, D5S209, and D5S210, which map to 5q31.3----q33.3. The Treacher Collins syndrome locus was linked closest to locus D5S210, which is associated with microsatellite polymorphisms, with a maximum lod score of 8.65 at theta = 0.02. The Treacher Collins syndrome locus was excluded from locus ADRB2R, which maps to 5q31----q32, and loci D5S22, D5S61, and D5S43, which map to 5q34----qter. There was no evidence for genetic heterogeneity among eight families with variable expression of the condition.

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Year:  1991        PMID: 1765376

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  11 in total

1.  The gene for an inherited form of deafness maps to chromosome 5q31.

Authors:  P E Leon; H Raventos; E Lynch; J Morrow; M C King
Journal:  Proc Natl Acad Sci U S A       Date:  1992-06-01       Impact factor: 11.205

2.  The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon.

Authors:  S J Edwards; A J Gladwin; M J Dixon
Journal:  Am J Hum Genet       Date:  1997-03       Impact factor: 11.025

Review 3.  Treacher Collins syndrome.

Authors:  M J Dixon
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

4.  Narrowing the position of the Treacher Collins syndrome locus to a small interval between three new microsatellite markers at 5q32-33.1.

Authors:  M J Dixon; J Dixon; T Houseal; M Bhatt; D C Ward; K Klinger; G M Landes
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

5.  A YAC contig encompassing the Treacher Collins syndrome critical region at 5q31.3-32.

Authors:  J Dixon; A J Gladwin; S K Loftus; J H Riley; R Perveen; J J Wasmuth; R Anand; M J Dixon
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

6.  TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.

Authors:  C A Wise; L C Chiang; W A Paznekas; M Sharma; M M Musy; J A Ashley; M Lovett; E W Jabs
Journal:  Proc Natl Acad Sci U S A       Date:  1997-04-01       Impact factor: 11.205

7.  Prenatal diagnosis in Treacher Collins syndrome using combined linkage analysis and ultrasound imaging.

Authors:  S J Edwards; A Fowlie; M P Cust; D T Liu; I D Young; M J Dixon
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

8.  The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.

Authors:  Benigno C Valdez; Dale Henning; Rolando B So; Jill Dixon; Michael J Dixon
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-12       Impact factor: 11.205

9.  Cytogenetic and clinical assessment of a family with treacher collins syndrome.

Authors:  Manoj Kumar; Rakesh Kumar; Mukesh Tanwar; Supriyo Ghose; Jasbir Kaur; Rima Dada
Journal:  Case Rep Med       Date:  2011-06-23

10.  PCR-based microsatellite polymorphisms in the detection of loss of heterozygosity in fresh and archival tumour tissue.

Authors:  N A Gruis; E C Abeln; A F Bardoel; P Devilee; R R Frants; C J Cornelisse
Journal:  Br J Cancer       Date:  1993-08       Impact factor: 7.640

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