These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 31901040)

  • 1. [Genetic analysis of a family of Van der Woude syndrome].
    Xu Y; Qian Y; Yao W; Dong M
    Zhejiang Da Xue Xue Bao Yi Xue Ban; 2019 Jun; 48(4):378-383. PubMed ID: 31901040
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Van der Woude and Popliteal Pterygium Syndromes: Broad intrafamilial variability in a three generation family with mutation in IRF6.
    Busche A; Hehr U; Sieg P; Gillessen-Kaesbach G
    Am J Med Genet A; 2016 Sep; 170(9):2404-7. PubMed ID: 27286731
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A clinical and multi‑omics study of Van der Woude syndrome in three generations of a Chinese family.
    Yang K; Dong XY; Wu J; Zhu JJ; Tan Y; Yan YS; Lin L; Zhang DL
    Mol Med Rep; 2020 Oct; 22(4):2925-2931. PubMed ID: 32945398
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Van der Woude Syndrome: IRF6 Mutations.
    Sunny AP; Arunachal G; Danda S
    Indian J Pediatr; 2019 Nov; 86(11):1070-1071. PubMed ID: 31468312
    [No Abstract]   [Full Text] [Related]  

  • 5. A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family With Van der Woude Syndrome.
    Tan EC; Lim HW; Lim ECP; Lee ST
    Cleft Palate Craniofac J; 2017 Jul; 54(4):442-445. PubMed ID: 27243668
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Search for genetic modifiers of IRF6 and genotype-phenotype correlations in Van der Woude and popliteal pterygium syndromes.
    Leslie EJ; Mancuso JL; Schutte BC; Cooper ME; Durda KM; L'Heureux J; Zucchero TM; Marazita ML; Murray JC
    Am J Med Genet A; 2013 Oct; 161A(10):2535-2544. PubMed ID: 23949966
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel mutation in the IRF6 gene associated with facial asymmetry in a family affected with Van der Woude syndrome.
    Miñones-Suárez L; Mas-Vidal A; Fernandez-Toral J; Llano-Rivas I; González-García M
    Pediatr Dermatol; 2012; 29(6):768-70. PubMed ID: 21995291
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel Mutations in the IRF6 Gene on the Background of Known Polymorphisms in Polish Patients With Orofacial Clefting.
    Charzewska A; Obersztyn E; Hoffman-Zacharska D; Lenart J; Poznański J; Bal J
    Cleft Palate Craniofac J; 2015 Sep; 52(5):e161-7. PubMed ID: 25489771
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered regulation of cell migration in IRF6-mutated orofacial cleft patients-derived primary cells reveals a novel role of Rho GTPases in cleft/lip palate development.
    Ghassibe-Sabbagh M; El Hajj J; Al Saneh M; El Baba N; Abou Issa J; Al Haddad M; El Atat O; Sabbagh J; Abou Chebel N; El-Sibai M
    Cells Dev; 2021 Jun; 166():203674. PubMed ID: 33994351
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [IRF6 gene mutation analysis in a van Der Woude syndrome family in Henan province].
    Wang XF; Xiao MZ; Shi JN; Zhang HB; Hu LD; Kong XY
    Shanghai Kou Qiang Yi Xue; 2005 Jun; 14(3):234-7. PubMed ID: 15995766
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Van-der-Woude Syndrome].
    Del Frari B; Amort M; Janecke AR; Schutte BC; Piza-Katzer H
    Klin Padiatr; 2008; 220(1):26-8. PubMed ID: 18095255
    [TBL] [Abstract][Full Text] [Related]  

  • 12. IRF6 mutations may not be a major cause of Van der Woude syndrome in India.
    Moghe GA; Mauli S
    Eur J Pediatr; 2011 Jan; 170(1):129. PubMed ID: 20845047
    [No Abstract]   [Full Text] [Related]  

  • 13. Van der Woude Syndrome With a Novel Mutation in the IRF6 Gene.
    Ural A; Bilgen F; Çakmakli S; Bekerecioğlu M
    J Craniofac Surg; 2019 Jul; 30(5):e465-e467. PubMed ID: 31299817
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparative analysis of IRF6 variants in families with Van der Woude syndrome and popliteal pterygium syndrome using public whole-exome databases.
    Leslie EJ; Standley J; Compton J; Bale S; Schutte BC; Murray JC
    Genet Med; 2013 May; 15(5):338-44. PubMed ID: 23154523
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel lip pit phenotypes and mutations of IRF6 in Van der Woude syndrome patients from Pakistan.
    Malik S; Wilcox ER; Naz S
    Clin Genet; 2014 May; 85(5):487-91. PubMed ID: 23713753
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Non-random distribution of deleterious mutations in the DNA and protein-binding domains of IRF6 are associated with Van Der Woude syndrome.
    Alade AA; Buxo-Martinez CJ; Mossey PA; Gowans LJJ; Eshete MA; Adeyemo WL; Naicker T; Awotoye WA; Adeleke C; Busch T; Toraño AM; Bello CA; Soto M; Soto M; Ledesma R; Marquez M; Cordero JF; Lopez-Del Valle LM; Salcedo MI; Debs N; Li M; Petrin A; Olotu J; Aldous C; Olutayo J; Ogunlewe MO; Abate F; Hailu T; Muhammed I; Gravem P; Deribew M; Gesses M; Hassan M; Pape J; Adeniyan OA; Obiri-Yeboah S; Arthur FKN; Oti AA; Olatosi O; Miller SE; Donkor P; Dunnwald MM; Marazita ML; Adeyemo AA; Murray JC; Butali A
    Mol Genet Genomic Med; 2020 Aug; 8(8):e1355. PubMed ID: 32558391
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Clinical and genetic features of Chinese kindreds with Van der Woude syndrome caused by interferon regulatory factor 6 mutation].
    Du XY; Li XY; Wu B; Xie C; Tian WD
    Hua Xi Kou Qiang Yi Xue Za Zhi; 2018 Dec; 36(6):623-627. PubMed ID: 30593107
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association between genotype and phenotype of virulence gene in Van der Woude syndrome families.
    Li S; Zhang X; Chen D; Zhao W; Zhang X; Jiao J; Guo L; Yin L; Song X; Liang C; Sun C
    Mol Med Rep; 2018 Jan; 17(1):1241-1246. PubMed ID: 29115498
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
    Pegelow M; Koillinen H; Magnusson M; Fransson I; Unneberg P; Kere J; Karsten A; Peyrard-Janvid M
    Cleft Palate Craniofac J; 2014 Jan; 51(1):49-55. PubMed ID: 23394314
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Microdeletion of the entire IRF6 gene in a Subsaharian African's family with Van der Woude syndrome.
    Mbuyi-Musanzayi S; Kasamba EI; Revencu N; Lukusa PT; Kalenga PM; Tshilombo FK; Reychler H; Devriendt K
    Clin Dysmorphol; 2020 Jan; 29(1):24-27. PubMed ID: 30946036
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.