Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome
Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses
Novel insertion in exon 5 of the TCOF1 gene in twin sisters with Treacher Collins syndrome | SpringerLink
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome - ScienceDirect
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome | Genetics in Medicine
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 | Genetics in Medicine
Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders
TCOF1 gene with newly identified and previously reported mutations. The... | Download Scientific Diagram
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Schematic view of chromosome 5 where the TCOF1 gene is located in the... | Download Scientific Diagram
Characterization of the Nucleolar Gene Product, Treacle, in Treacher Collins Syndrome | Molecular Biology of the Cell
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome