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 *

204 related articles for article (PubMed ID: 15163158)

  • 81. Congenital bilateral lower lip pits associated with fistulae of the minor salivary glands: case report of the principal Van der Woude syndrome's trait.
    Souto LR
    Aesthetic Plast Surg; 2008 Jan; 32(1):172-4. PubMed ID: 17805920
    [TBL] [Abstract][Full Text] [Related]  

  • 82. Median cleft of the lower lip associated with lip pits and cleft of the lip and palate.
    Lo LJ; Noordhoff MS
    Cleft Palate Craniofac J; 1999 Jan; 36(1):86-7. PubMed ID: 10067768
    [No Abstract]   [Full Text] [Related]  

  • 83. Microdeletions at chromosome bands 1q32-q41 as a cause of Van der Woude syndrome.
    Schutte BC; Basart AM; Watanabe Y; Laffin JJ; Coppage K; Bjork BC; Daack-Hirsch S; Patil S; Dixon MJ; Murray JC
    Am J Med Genet; 1999 May; 84(2):145-50. PubMed ID: 10323740
    [TBL] [Abstract][Full Text] [Related]  

  • 84. Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome.
    Knight AS; Schutte BC; Jiang R; Dixon MJ
    Dev Dyn; 2006 May; 235(5):1441-7. PubMed ID: 16245336
    [TBL] [Abstract][Full Text] [Related]  

  • 85. Congenital lower lip pits (van der Woude syndrome): what pathologists need to know.
    Fan R; Flores RL; Faught PR; Lin J
    Pediatr Dev Pathol; 2013; 16(5):343-7. PubMed ID: 23947719
    [TBL] [Abstract][Full Text] [Related]  

  • 86. The Van der Woude syndrome (dominantly inherited lip pits and clefts).
    Schinzel A; Kläusler M
    J Med Genet; 1986 Aug; 23(4):291-4. PubMed ID: 3746828
    [No Abstract]   [Full Text] [Related]  

  • 87. 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]  

  • 88. An alternative technique using a gutta percha points and blue methylene to excision of congenital fistula of lower lip in patient with Van der Woude syndrome.
    Castro CH; De Carvalho MF; Veloso DC; De Moraes M
    Stomatologija; 2012; 14(2):60-4. PubMed ID: 23037784
    [TBL] [Abstract][Full Text] [Related]  

  • 89. 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]  

  • 90. Novel mutations in the IRF6 gene for Van der Woude syndrome.
    Wang X; Liu J; Zhang H; Xiao M; Li J; Yang C; Lin X; Wu Z; Hu L; Kong X
    Hum Genet; 2003 Oct; 113(5):382-6. PubMed ID: 12920575
    [TBL] [Abstract][Full Text] [Related]  

  • 91. 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]  

  • 92. Identification of novel mutations of IRF6 gene in Chinese families with Van der Woude syndrome.
    Ye XQ; Jin HX; Shi LS; Fan MW; Song GT; Fan HL; Bian Z
    Int J Mol Med; 2005 Nov; 16(5):851-6. PubMed ID: 16211254
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Possible relationship between the van der Woude syndrome (vWS) locus and nonsyndromic cleft lip with or without cleft palate (NSCL/P).
    Houdayer C; Bonaïti-Pellié C; Erguy C; Soupre V; Dondon MG; Bürglen L; Cougoureux E; Couderc R; Vazquez MP; Bahuau M
    Am J Med Genet; 2001 Nov; 104(1):86-92. PubMed ID: 11746036
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Van der Woude syndrome.
    Kulkarni ML; Sureshkumar C; Venkataramana V
    Ann Dent; 1995; 54(1-2):34-5. PubMed ID: 8572542
    [No Abstract]   [Full Text] [Related]  

  • 95. Confirmation of linkage of Van der Woude syndrome to chromosome 1q32: evidence of association with STR alleles suggests possible unique origin of the disease mutation.
    Beiraghi S; Miller-Chisholm A; Kimberling WJ; Sun CE; Wang YF; Russell LJ; Khoshnevisan M; Storm AL; Long RE; Witt PD; Mazaheri M; Diehl SR
    J Craniofac Genet Dev Biol; 1999; 19(3):128-34. PubMed ID: 10589394
    [TBL] [Abstract][Full Text] [Related]  

  • 96. 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]  

  • 97. 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]  

  • 98. 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]  

  • 99. Popliteal pterygium syndrome: a clinical study of three families and report of linkage to the Van der Woude syndrome locus on 1q32.
    Lees MM; Winter RM; Malcolm S; Saal HM; Chitty L
    J Med Genet; 1999 Dec; 36(12):888-92. PubMed ID: 10593995
    [TBL] [Abstract][Full Text] [Related]  

  • 100. 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]  

    [Previous]   [Next]    [New Search]
    of 11.