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 *

302 related articles for article (PubMed ID: 29708799)

  • 21. 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]  

  • 22. Lower lip pits in a patient with van der Woude syndrome.
    Baghestani S; Sadeghi N; Yavarian M; Alghasi H
    J Craniofac Surg; 2010 Sep; 21(5):1380-1. PubMed ID: 20818247
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [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]  

  • 24. [Van der Woude syndrome: An unrecognised clinical entity].
    Abbo O; Vaysse F; Bieth E; Galinier P
    Ann Chir Plast Esthet; 2014 Feb; 59(1):81-4. PubMed ID: 22014507
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Van der Woude and Popliteal Pterygium Syndromes.
    Bennun RD; Stefano E; Moggi LE
    J Craniofac Surg; 2018 Sep; 29(6):1434-1436. PubMed ID: 29916977
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [THE PIERRE ROBIN SYNDROME (MICROGNATHIA, CLEFT PALATE, GLOSSOPTOSIS)].
    CALVANI M; TADDEINI R
    Pediatria (Napoli); 1963; 71():669-90. PubMed ID: 14051039
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Case report of Pierre Robin sequence with severe upper airway obstruction who was rescued by fiberoptic nasotracheal intubation.
    Takeshita S; Ueda H; Goto T; Muto D; Kakita H; Oshima K; Tainaka T; Ono T; Kazaoka Y; Yamada Y
    BMC Anesthesiol; 2017 Mar; 17(1):43. PubMed ID: 28288578
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic heterogeneity in Van der Woude syndrome: identification of NOL4 and IRF6 haplotype from the noncoding region as candidates in two families.
    Kumari PK; Ali A; Singh SK; Chaurasia A; Raman R
    J Genet; 2018 Mar; 97(1):275-285. PubMed ID: 29666346
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Cognitive dysfunction in adults with Van der Woude syndrome.
    Nopoulos P; Richman L; Andreasen N; Murray JC; Schutte B
    Genet Med; 2007 Apr; 9(4):213-8. PubMed ID: 17438385
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.
    Manjegowda DS; Prasad M; Veerappa AM; Ramachandra NB
    Genet Res (Camb); 2014 Oct; 96():e12. PubMed ID: 25579819
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Mutations in Van Der Woude Families From Ethiopia.
    Eshete M; Alade A; Abate F; Mossey PA; Awotoye WA; Busch T; Hailu A; Demissie Y; Butali A
    J Craniofac Surg; 2022 Mar-Apr 01; 33(2):e138-e140. PubMed ID: 34643600
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel IRF6 Mutations Detected in Orofacial Cleft Patients by Targeted Massively Parallel Sequencing.
    Khandelwal KD; Ishorst N; Zhou H; Ludwig KU; Venselaar H; Gilissen C; Thonissen M; van Rooij IA; Dreesen K; Steehouwer M; van de Vorst M; Bloemen M; van Beusekom E; Roosenboom J; Borstlap W; Admiraal R; Dormaar T; Schoenaers J; Vander Poorten V; Hens G; Verdonck A; Bergé S; Roeleveldt N; Vriend G; Devriendt K; Brunner HG; Mangold E; Hoischen A; van Bokhoven H; Carels CE
    J Dent Res; 2017 Feb; 96(2):179-185. PubMed ID: 27834299
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Van der Woude syndrome with an unusual intraoral finding.
    Sarode GS; Desai RS; Sarode SC; Kulkarni MA
    Indian J Dent Res; 2011; 22(1):164-5. PubMed ID: 21525698
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
    Peyrard-Janvid M; Leslie EJ; Kousa YA; Smith TL; Dunnwald M; Magnusson M; Lentz BA; Unneberg P; Fransson I; Koillinen HK; Rautio J; Pegelow M; Karsten A; Basel-Vanagaite L; Gordon W; Andersen B; Svensson T; Murray JC; Cornell RA; Kere J; Schutte BC
    Am J Hum Genet; 2014 Jan; 94(1):23-32. PubMed ID: 24360809
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Novel IRF6 mutations in Honduran Van der Woude syndrome patients.
    Birkeland AC; Larrabee Y; Kent DT; Flores C; Su GH; Lee JH; Haddad J
    Mol Med Rep; 2011; 4(2):237-41. PubMed ID: 21468557
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical attitude to the patient with Non-syndromic Pierre Robin Sequence with the cleft of soft palate and uvula - The necessity of fibroscopic investigation.
    Koukouvitaki M; Arkoumanis PT; Brucknerova J; Brucknerova I
    Neuro Endocrinol Lett; 2019 Mar; 40(1):5-9. PubMed ID: 31184816
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Identification of IRF6 gene variants in three families with Van der Woude syndrome.
    Tan EC; Lim EC; Yap SH; Lee ST; Cheng J; Por YC; Yeow V
    Int J Mol Med; 2008 Jun; 21(6):747-51. PubMed ID: 18506368
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.