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Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome

POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4  | Genetics in Medicine
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 | Genetics in Medicine

Patients with TCS and detected TCOF1 mutation, (a-k) are arranged... |  Download Scientific Diagram
Patients with TCS and detected TCOF1 mutation, (a-k) are arranged... | Download Scientific Diagram

Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for  Treacher Collins syndrome with intellectual disability | European Journal  of Human Genetics
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability | European Journal of Human Genetics

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

Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA  damage response | PNAS
Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response | PNAS

The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal  DNA gene transcription by interacting with upstream binding factor | PNAS
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS

TCOF1 gene with newly identified and previously reported mutations. The...  | Download Scientific Diagram
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
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
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome

Rare syndromes of the head and face: mandibulofacial and acrofacial  dysostoses - Terrazas - 2017 - WIREs Developmental Biology - Wiley Online  Library
Rare syndromes of the head and face: mandibulofacial and acrofacial dysostoses - Terrazas - 2017 - WIREs Developmental Biology - Wiley Online Library

Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial  Dysostoses
Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses

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
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

TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody

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
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

The Role of Mutations on Gene TCOF1, in Treacher Collins Syndrome | PDF
The Role of Mutations on Gene TCOF1, in Treacher Collins Syndrome | PDF

Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA  damage response | PNAS
Treacher Collins syndrome TCOF1 protein cooperates with NBS1 in the DNA damage response | PNAS

Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial  Neural Crest Cell Development and the Phenotype Variability of Craniofacial  Disorders
Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome  patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley  Online Library
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library

Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial  Dysostoses
Frontiers | Targeted Next-Generation Sequencing in the Diagnosis of Facial Dysostoses

Primers self-designed for TCOF1 gene amplification and sequencing |  Download Table
Primers self-designed for TCOF1 gene amplification and sequencing | Download Table

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
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

Phenotype Analysis and Genetic Study of Chinese Patients With Treacher  Collins Syndrome - Meng Lu, Bin Yang, Zixiang Chen, Haiyue Jiang, Bo Pan,  2022
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

Partial sequencing of the TCOF1 gene. The patient carries a novel... |  Download Scientific Diagram
Partial sequencing of the TCOF1 gene. The patient carries a novel... | Download Scientific Diagram

Gross deletions in TCOF1 are a cause of Treacher–Collins–Franceschetti  syndrome | European Journal of Human Genetics
Gross deletions in TCOF1 are a cause of Treacher–Collins–Franceschetti syndrome | European Journal of Human Genetics