The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS
TCOF1 antibody (11003-1-AP) | Proteintech
Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response | PNAS
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome | Human Genome Variation
Schematic view of chromosome 5 where the TCOF1 gene is located in the... | Download Scientific Diagram
Phenotype and analysis of the amplified fragment of exon 13 of the... | Download Scientific Diagram
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Figure 7 from The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome | Genetics in Medicine
TCOF1 Polyclonal Antibody (PA5-58309)
Partial sequencing of the TCOF1 gene. The patient carries a novel... | Download Scientific Diagram
TRF2 recruits nucleolar protein TCOF1 to coordinate telomere transcription and replication | Cell Death & Differentiation
Novel autosomal dominant mandibulofacial dysostosis with ptosis: clinical description and exclusion of TCOF1 | Journal of Medical Genetics
Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation | European Journal of Human Genetics
Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response | PNAS
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability | European Journal of Human Genetics
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
Anti-TCOF1 Antibody (CAB2512) | WB
TCOF1 pathogenic variants identified by Whole-exome sequencing in Chinese Treacher Collins syndrome families and hearing rehabilitation effect | Orphanet Journal of Rare Diseases | Full Text
Individuals with TCS and detected TCOF1 mutation Reprinted by... | Download Scientific Diagram
Treacher Collins syndrome: a clinical and molecular study based on a large series of patients | Genetics in Medicine
