BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 37640998)

  • 1. [
    Li Y; Chi W; Lin K; Zu J; Shao H; Mao Z; Chen Q; Ma J
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2023 Sep; 37(9):748-754. PubMed ID: 37640998
    [No Abstract]   [Full Text] [Related]  

  • 2. TCOF1 pathogenic variants identified by Whole-exome sequencing in Chinese Treacher Collins syndrome families and hearing rehabilitation effect.
    Fan X; Wang Y; Fan Y; Du H; Luo N; Zhang S; Chen X
    Orphanet J Rare Dis; 2019 Jul; 14(1):178. PubMed ID: 31307516
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients.
    Zhang C; An L; Xue H; Hao S; Yan Y; Zhang Q; Jin X; Li Q; Zhou B; Feng X; Ma P; Wang X; Chen X; Chen C; Cao Z; Ma X
    J Clin Lab Anal; 2021 Jan; 35(1):e23567. PubMed ID: 32909271
    [TBL] [Abstract][Full Text] [Related]  

  • 4. De novo TCOF1 mutation in Treacher Collins syndrome.
    Liu J; Dong J; Li P; Duan W
    Int J Pediatr Otorhinolaryngol; 2021 Aug; 147():110765. PubMed ID: 34058530
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Treacher Collins syndrome: A novel TCOF1 mutation and monopodial stapes.
    Kantaputra PN; Tripuwabhrut K; Intachai W; Carlson BM; Quarto N; Ngamphiw C; Tongsima S; Sonsuwan N
    Clin Otolaryngol; 2020 Sep; 45(5):695-702. PubMed ID: 32351010
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Missense Variant in the
    Yin B; Pang YY; Shi JY; Lin YS; Sun JL; Zheng Q; Shi B; Jia ZL
    Cleft Palate Craniofac J; 2024 Feb; 61(2):192-199. PubMed ID: 36082953
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in the TCOF1 gene found in two Chinese cases of Treacher Collins syndrome.
    Zhang X; Fan Y; Zhang Y; Xue H; Chen X
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1410-5. PubMed ID: 23838542
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel nonsense mutation in the TCOF1 gene in one Chinese newborn with Treacher Collins syndrome.
    Zeng H; Xie M; Li J; Xie H; Lu X
    Int J Pediatr Otorhinolaryngol; 2021 Feb; 141():110561. PubMed ID: 33341718
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of TCOF1 mutation in a Chinese patient with Treacher-Collins syndrome].
    Huang H; Yang Y; Wu X; Duan J; Li H; Yi L; Fu J; Guo Z; Yue P; Li W; Zhang X; Huo X; Chen K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Oct; 35(5):683-685. PubMed ID: 30298495
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations.
    Chen Y; Guo L; Li CL; Shan J; Xu HS; Li JY; Sun S; Hao SJ; Jin L; Chai G; Zhang TY
    Mol Genet Genomics; 2018 Apr; 293(2):569-577. PubMed ID: 29230583
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Clinical and genetic analysis of a patient with Treacher Collins syndrome in TCOF1 gene].
    Li H; Zhang X; Li Z; Chen J; Lu Y; Jia J; Yuan H; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 May; 26(10):459-62. PubMed ID: 22870720
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome.
    Liu J; Lin P; Pang J; Jia Z; Peng Y; Xi H; Wu L; Li Z; Wang H
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1313. PubMed ID: 32543076
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Large deletions encompassing the TCOF1 and CAMK2A genes are responsible for Treacher Collins syndrome with intellectual disability.
    Vincent M; Collet C; Verloes A; Lambert L; Herlin C; Blanchet C; Sanchez E; Drunat S; Vigneron J; Laplanche JL; Puechberty J; Sarda P; Geneviève D
    Eur J Hum Genet; 2014 Jan; 22(1):52-6. PubMed ID: 23695276
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.
    Su PH; Chen JY; Chen SJ; Yu JS
    J Formos Med Assoc; 2006 Jun; 105(6):518-21. PubMed ID: 16801042
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.
    Conte C; D'Apice MR; Rinaldi F; Gambardella S; Sangiuolo F; Novelli G
    BMC Med Genet; 2011 Sep; 12():125. PubMed ID: 21951868
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome.
    Hao S; Jin L; Wang H; Li C; Zheng F; Ma D; Zhang T
    J Craniofac Surg; 2016 Sep; 27(6):e583-6. PubMed ID: 27526242
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Treacher Collins Syndrome: Genetics, Clinical Features and Management.
    Marszałek-Kruk BA; Wójcicki P; Dowgierd K; Śmigiel R
    Genes (Basel); 2021 Sep; 12(9):. PubMed ID: 34573374
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [The research progress of Treacher Collins syndrome].
    Wang P; Fan X; Fan Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Feb; 30(4):333-8. PubMed ID: 27373049
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients.
    Masotti C; Ornelas CC; Splendore-Gordonos A; Moura R; Félix TM; Alonso N; Camargo AA; Passos-Bueno MR
    BMC Med Genet; 2009 Dec; 10():136. PubMed ID: 20003452
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 9.