Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons
- 17 March 2004
- Vol. 328, 49-57
- https://doi.org/10.1016/j.gene.2003.11.027
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Proteomic Analysis of Human Nop56p-associated Pre-ribosomal Ribonucleoprotein ComplexesJournal of Biological Chemistry, 2003
- Mutation testing in Treacher Collins SyndromeJournal of Orthodontics, 2002
- Canine TCOF1; cloning, chromosome assignment and genetic analysis in dogs with different head typesMammalian Genome, 2001
- Increased levels of apoptosis in the prefusion neural folds underlie the craniofacial disorder, Treacher Collins syndromeHuman Molecular Genetics, 2000
- Sequence Analysis, Identification of Evolutionary Conserved Motifs and Expression Analysis of Murine tcof1 Provide Further Evidence for a Potential Function for the Gene and Its Human Homologue, TCOF1Human Molecular Genetics, 1997
- Identification of the complete coding sequence and genomic organization of the Treacher Collins syndrome gene.Genome Research, 1997
- Treacher Collins syndrome may result from insertions, deletions or splicing mutations, which introduce a termination codon into the geneHuman Molecular Genetics, 1996
- Protein Sequence Requirements for Function of the Human T-Cell Leukemia Virus Type 1 Rex Nuclear Export Signal Delineated by a Novel In Vivo Randomization-Selection AssayMolecular and Cellular Biology, 1996
- Nuclear targeting sequences — a consensus?Trends in Biochemical Sciences, 1991
- Mandibulo-Facial DysostosisAmerican Journal of Diseases of Children, 1967