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Journal Abstract Search

243 related items for PubMed ID: 3367915

  • 1. [Van der Woude syndrome in combination with ring chromosome 18].
    Kalker U, Gabriel M, Jacobi G.
    Monatsschr Kinderheilkd; 1988 Feb; 136(2):95-8. PubMed ID: 3367915
    [Abstract] [Full Text] [Related]

  • 2. Phenotypic variability in van der Woude syndrome.
    Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.
    Genet Couns; 1995 Feb; 6(3):221-6. PubMed ID: 8588850
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  • 3. The penetrance and variable expression of the Van der Woude syndrome: implications for genetic counseling.
    Shprintzen RJ, Goldberg RB, Sidoti EJ.
    Cleft Palate J; 1980 Jan; 17(1):52-7. PubMed ID: 6928118
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  • 5. [Ectodactylia-ectodermal dysplasia, cleft lip, jaw and palate syndrome (EEC syndrome). Association with van der Woude syndrome?].
    Haensch R, Küster W, Hammerstein W.
    Dtsch Z Mund Kiefer Gesichtschir; 1985 Jan; 9(3):225-6. PubMed ID: 3868444
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  • 6. Van der Woude syndrome with mental retardation: case report.
    Ugwu BT, Momoh JT.
    East Afr Med J; 2001 Feb; 78(2):111-2. PubMed ID: 11682943
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  • 9. 4p- syndrome and 9p tetrasomy mosaicism with cleft lip and palate.
    Kobayashi J, Kimijima Y, Yamada S, Amagasa T, Saito-Ohara F.
    J Craniomaxillofac Surg; 2000 Jun; 28(3):165-70. PubMed ID: 10964553
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  • 11. Isolated lower lip fistulas in Van der Woude syndrome.
    Etöz OA, Etöz A.
    J Craniofac Surg; 2009 Sep; 20(5):1612-4. PubMed ID: 19816310
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  • 12. Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.
    Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J.
    Eur J Hum Genet; 2001 Oct; 9(10):747-52. PubMed ID: 11781685
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  • 13. [Analysis of genetic penetrance in the pedigree of cases with Van der Woude syndrome: report of five cases].
    Bozkurt M, Kapı E, Külahçı Y, Zor F, Benlier E, Balkan M, Kılınç N, Imirzalıoğlu N, Kuvat SV.
    Kulak Burun Bogaz Ihtis Derg; 2010 Oct; 20(4):200-4. PubMed ID: 20626329
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  • 14. Report of two cases with Van der Woude syndrome: a child and her mother.
    Koçer U, Aksoy HM, Tiftikcioğlu YO, Cöloğlu H, Karaaslan O.
    Genet Couns; 2001 Oct; 12(4):341-6. PubMed ID: 11837602
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  • 15. 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 Oct; 28(2):104-9. PubMed ID: 20660977
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  • 16. Van der Woude syndrome: dentofacial features and implications for clinical practice.
    Lam AK, David DJ, Townsend GC, Anderson PJ.
    Aust Dent J; 2010 Mar; 55(1):51-8. PubMed ID: 20415912
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  • 17. [Congenital paramedian lip fistulas].
    Wirth H, Tilgen W.
    Hautarzt; 1980 Nov; 31(11):610-2. PubMed ID: 7451144
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  • 18. The 18q deletion syndrome and analysis of the critical region for orofacial cleft at 18q22.3.
    Dostal A, Nemeckova J, Gaillyova R.
    J Craniomaxillofac Surg; 2009 Jul; 37(5):272-5. PubMed ID: 19157891
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  • 19. [The functional and surgical rehabilitative treatment of cleft lip and cleft palate in a case of the syndrome of the deletion of the long arm of chromosome 18 diagnosed in utero].
    Casseler F, Radovich F, Guidetti F.
    Minerva Stomatol; 1991 Jul; 40(7-8):515-20. PubMed ID: 1753934
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  • 20. Van der Woude syndrome: a case report.
    Arangannal P, Muthu MS, Nirmal L.
    J Indian Soc Pedod Prev Dent; 2002 Sep; 20(3):102-3. PubMed ID: 12435007
    [Abstract] [Full Text] [Related]

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