Associated Papers
Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.
Bowman M et al.
European Journal of Human Genetics : Ejhg, 2012
TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature.
Splendore A et al.
Human Mutation, 2005
Identification of mutations in TCOF1: use of molecular analysis in the pre- and postnatal diagnosis of Treacher Collins syndrome.
Dixon J et al.
American Journal of Medical Genetics. Part A, 2004
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