IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Phenotype and analysis of the amplified fragment of exon 13 of the... | Download Scientific Diagram
Phenotype Analysis and Genetic Study of Chinese Patients With Treacher Collins Syndrome - Meng Lu, Bin Yang, Zixiang Chen, Haiyue Jiang, Bo Pan, 2022
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
The Role of Mutations on Gene TCOF1, in Treacher Collins Syndrome | PDF
Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome | Human Genome Variation
TCOF1 gene with newly identified and previously reported mutations. The... | Download Scientific Diagram
Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses
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
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Partial sequencing of the TCOF1 gene. The patient carries a novel... | Download Scientific Diagram
Another face of the Treacher Collins syndrome (TCOF1) gene: identification of additional exons - ScienceDirect
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region | PNAS
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome - ScienceDirect
PDF] The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
Schematic view of chromosome 5 where the TCOF1 gene is located in the... | Download Scientific Diagram
A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome - ScienceDirect
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
Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses
The Role of Mutations on Gene TCOF1, in Treacher Collins Syndrome | PDF
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody