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