Patients with TCS and detected TCOF1 mutation, (a-k) are arranged... | Download Scientific Diagram
Identification of a novel TCOF1 mutation in a Chinese family with Treacher Collins syndrome
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
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome
Phenotype Analysis and Genetic Study of Chinese Patients With Treacher Collins Syndrome - Meng Lu, Bin Yang, Zixiang Chen, Haiyue Jiang, Bo Pan, 2022
Novel mutation in the TCOF1 gene in a patient with Treacher Collins syndrome - ScienceDirect
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library
TCOF1 gene with newly identified and previously reported mutations. The... | Download Scientific Diagram
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 | Genetics in Medicine
TCOF1 Gene (Treacle Ribosome Biogenesis Factor 1) - StoryMD
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library
Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome | Human Genome Variation
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
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
Treacher Collins Syndrome - Brianna Howland - YouTube
Face off against ROS: Tcof1/Treacle safeguards neuroepithelial cells and progenitor neural crest cells from oxidative stress during craniofacial development - Sakai - 2016 - Development, Growth & Differentiation - Wiley Online Library
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability | European Journal of Human Genetics
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
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
