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 *

124 related articles for article (PubMed ID: 38861357)

  • 21. Surgical management of lower lip pits in Van der Woude syndrome.
    Bertin H; Diallo-Hornez G; Isidor B; Mercier J
    J Stomatol Oral Maxillofac Surg; 2018 Feb; 119(1):67-70. PubMed ID: 28893716
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Congenital lip pits and van der Woude syndrome.
    Ziai MN; Benson AG; Djalilian HR
    J Craniofac Surg; 2005 Sep; 16(5):930-2. PubMed ID: 16192885
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. Genetic analysis in families with van der Woude syndrome.
    Burdick AB; Bixler D; Puckett CL
    J Craniofac Genet Dev Biol; 1985; 5(2):181-208. PubMed ID: 4019732
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Lower lip pits: van der woude or kabuki syndrome?
    David-Paloyo FP; Yang X; Lin JL; Wong FH; Wu-Chou YH; Lo LJ
    Cleft Palate Craniofac J; 2014 Nov; 51(6):729-34. PubMed ID: 24088119
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel IRF6 mutations in Chinese patients with Van der Woude syndrome.
    Du X; Tang W; Tian W; Li S; Li X; Liu L; Zheng X; Chen X; Lin Y; Tang Y
    J Dent Res; 2006 Oct; 85(10):937-40. PubMed ID: 16998136
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Rare and Multiple Hypodontia in Van der Woude Syndrome: Case Report.
    Trevizan ACDS; Gonçales AGB; Centurion Pagin BS; Pagin O; Neves LTD
    Cleft Palate Craniofac J; 2023 Feb; 60(2):243-248. PubMed ID: 34787023
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A case of vander woude syndrome with rare phenotypic expressions.
    Tripathi A; Tiwari B; Gupta S; Patil R; Khanna V
    J Clin Diagn Res; 2014 Oct; 8(10):PD03-5. PubMed ID: 25478421
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Solitary congenital lip pit in an infant.
    Neale H; Blundell AR; Schmidt B; Hawryluk EB
    Pediatr Dermatol; 2021 Sep; 38(5):1363-1365. PubMed ID: 34346094
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The syndrome of pit of the lower lip and its association with cleft palate.
    Kaul B; Mahajan N; Gupta R; Kotwal B
    Contemp Clin Dent; 2014 Jul; 5(3):383-5. PubMed ID: 25191078
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Three novel mutations of the IRF6 gene with one associated with an unusual feature in Van der Woude syndrome.
    Yeetong P; Mahatumarat C; Siriwan P; Rojvachiranonda N; Suphapeetiporn K; Shotelersuk V
    Am J Med Genet A; 2009 Nov; 149A(11):2489-92. PubMed ID: 19842205
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Orofacial clefting: update on the role of genetics.
    Ghassibe M; Bayet B; Revencu N; Desmyter L; Verellen-Dumoulin C; Gillerot Y; Deggouj N; Vanwijck R; Vikkula M;
    B-ENT; 2006; 2 Suppl 4():20-4. PubMed ID: 17366841
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Bilateral congenital pits of the upper lip.
    Ozgür F; Tunçbilek G
    Ann Plast Surg; 2000 Dec; 45(6):658-61. PubMed ID: 11128769
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification of two novel mutations of IRF6 in Korean families affected with Van der Woude syndrome.
    Kim Y; Park JY; Lee TJ; Yoo HW
    Int J Mol Med; 2003 Oct; 12(4):465-8. PubMed ID: 12964020
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The role of 9qh+ in phenotypic and genotypic heterogeneity in a Van der Woude syndrome pedigree.
    Moghe GA; Kaur MS; Thomas AM; Raseswari T; Swapna M; Rao L
    J Indian Soc Pedod Prev Dent; 2010; 28(2):104-9. PubMed ID: 20660977
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [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]  

  • 37. [Van der Woude syndrome].
    Calzavara Pinton PG; Gavazzoni R; Carlino A; Leali C
    G Ital Dermatol Venereol; 1989 Apr; 124(4):171-3. PubMed ID: 2807397
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Dominantly inherited lower lip fistulas and facial clefts (Van der Woude syndrome). A study of 52 cases].
    Kläusler M; Schinzel A; Gnoinski W; Hotz M; Perko M
    Schweiz Med Wochenschr; 1987 Jan; 117(4):127-34. PubMed ID: 3823824
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Midline Congenital Upper Lip Sinus: A Rare Case.
    Chowdhary F; Chowdhary A; Chowdhary Z; Chowdhary A
    Indian J Otolaryngol Head Neck Surg; 2019 Oct; 71(Suppl 1):553-557. PubMed ID: 31742020
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A novel mutation, 1234del(C), of the IRF6 in a Thai family with Van der Woude syndrome.
    Shotelersuk V; Srichomthong C; Yoshiura K; Niikawa N
    Int J Mol Med; 2003 Apr; 11(4):505-7. PubMed ID: 12632105
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.