Generation of a human induced pluripotent stem cell line (PSHi002-A) from a Treacher-Collins syndrome patient carrying a TCOF1 gene mutation (c.1966_1969dup) - ScienceDirect
Partial sequencing of the TCOF1 gene. The patient carries a novel... | Download Scientific Diagram
Treacher Collins-Franceschetti Syndrome | Hereditary Ocular Diseases
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library
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
Clinical characteristics and segregation results of patient 2 (A-C)... | Download Scientific Diagram
![PDF] The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/f03f20fbaf8cd192eb0d7136310c89eadc413609/4-Figure3-1.png "PDF] The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar")
PDF] The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Novel mutation in the TCOF1 gene in a patient with Treacher Collins syndrome - ScienceDirect
Figure 5 from The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
A Novel Missense Variant in the TCOF1 Gene in one Chinese Case With Treacher Collins Syndrome - Bin Yin, Yu-Ya Pang, Jia-Yu Shi, Yan-Song Lin, Jia-Lin Sun, Qian Zheng, Bing Shi, Zhong-Lin
Treacher Collins syndrome - wikidoc
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library
The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome. - Abstract - Europe PMC
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome | Genetics in Medicine
Schematic view of chromosome 5 where the TCOF1 gene is located in the... | Download Scientific Diagram
TCOF1 gene with newly identified and previously reported mutations. 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
Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 | Genetics in Medicine
