Victimelor greu de multumit Distrage tcof1 gene mutation spațios balenă Gălbui
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
Patients with TCS and detected TCOF1 mutation, (a-k) are arranged... | Download Scientific Diagram
Novel mutation in the TCOF1 gene in a patient with Treacher Collins syndrome
The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome. - Abstract - Europe PMC
POLR1B and neural crest cell anomalies in Treacher Collins syndrome type 4 | Genetics in Medicine
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS
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
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
TCOF1 Gene - GeneCards | TCOF Protein | TCOF Antibody
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
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
Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability | European Journal of Human Genetics
A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome - ScienceDirect
PDF] The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
Partial sequencing of the TCOF1 gene. The patient carries a novel... | Download Scientific Diagram
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients - Zhang - 2021 - Journal of Clinical Laboratory Analysis - Wiley Online Library
The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor | PNAS
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
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome
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
First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome
Figure 5 from The Treacher Collins syndrome (TCOF1) gene product is involved in pre-rRNA methylation. | Semantic Scholar
Autosomal recessive POLR1D mutation with decrease of TCOF1 mRNA is responsible for Treacher Collins syndrome | Genetics in Medicine
Frontiers | Diabetes, Oxidative Stress, and DNA Damage Modulate Cranial Neural Crest Cell Development and the Phenotype Variability of Craniofacial Disorders
Identification of three novel TCOF1 mutations in patients with Treacher Collins Syndrome | Human Genome Variation
IJMS | Free Full-Text | The Role of TCOF1 Gene in Health and Disease: Beyond Treacher Collins Syndrome