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Journal Abstract Search

223 related items for PubMed ID: 6573981

  • 41. [Congenital paramedian lip fistulas].
    Wirth H, Tilgen W.
    Hautarzt; 1980 Nov; 31(11):610-2. PubMed ID: 7451144
    [Abstract] [Full Text] [Related]

  • 42. Cleft lip and/or palate in two cases of 46,X,i(Xq) Turner syndrome.
    Corona-Rivera JR, Corona-Rivera E, Bobadilla-Morales L, Garcia-Cobia TA, Corona-Rivera A.
    Genet Couns; 2002 Nov; 13(1):19-22. PubMed ID: 12017233
    [Abstract] [Full Text] [Related]

  • 43. Natal teeth in monozygotic twins with Van der Woude syndrome.
    Hersh JH, Verdi GD.
    Cleft Palate Craniofac J; 1992 May; 29(3):279-81. PubMed ID: 1591263
    [Abstract] [Full Text] [Related]

  • 44. [Van der Woude syndrome (lip pits, cleft lip and cleft palate syndrome)].
    Gao N.
    Zhonghua Zheng Xing Shao Shang Wai Ke Za Zhi; 1989 Jun; 5(2):98-9, 157. PubMed ID: 2509050
    [Abstract] [Full Text] [Related]

  • 45. Clinical and genetic study on 356 Brazilian patients with a distinct phenotype of cleft lip and palate without alveolar ridge involvement.
    Alvarez CW, Guion-Almeida ML, Richieri-Costa A.
    J Craniomaxillofac Surg; 2014 Dec; 42(8):1952-7. PubMed ID: 25441864
    [Abstract] [Full Text] [Related]

  • 46. Correlations of sinus, conical elevation, median depression of the lower lip and types of oral clefts.
    Ranta R.
    Int J Oral Surg; 1985 Dec; 14(6):479-84. PubMed ID: 3936795
    [Abstract] [Full Text] [Related]

  • 47. 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
    [Abstract] [Full Text] [Related]

  • 48. Distinct craniofacial syndrome of lagophthalmia and bilateral cleft lip and palate.
    Korula S, Wilson L, Salomonson J.
    Am J Med Genet; 1995 Nov 06; 59(2):229-33. PubMed ID: 8588591
    [Abstract] [Full Text] [Related]

  • 49. 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 06; 9(10):747-52. PubMed ID: 11781685
    [Abstract] [Full Text] [Related]

  • 50.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 51. 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 06; 12(4):465-8. PubMed ID: 12964020
    [Abstract] [Full Text] [Related]

  • 52. The van der Woude syndrome in a large kindred: variability, penetrance, genetic risks.
    Janku P, Robinow M, Kelly T, Bralley R, Baynes A, Edgerton MT.
    Am J Med Genet; 1980 Oct 06; 5(2):117-23. PubMed ID: 7395906
    [Abstract] [Full Text] [Related]

  • 53. [Population and familial incidence of orofacial anomalies considered microforms of cleft lip and palate].
    Demikova NS, Makarenkova LV.
    Genetika; 1983 Apr 06; 19(4):679-84. PubMed ID: 6222937
    [Abstract] [Full Text] [Related]

  • 54. A novel IRF6 nonsense mutation (Y67X) in a German family with Van der Woude syndrome.
    Brosch S, Baur M, Blin N, Reinert S, Pfister M.
    Int J Mol Med; 2007 Jul 06; 20(1):85-9. PubMed ID: 17549393
    [Abstract] [Full Text] [Related]

  • 55. [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 Jul 06; 20(4):200-4. PubMed ID: 20626329
    [Abstract] [Full Text] [Related]

  • 56. Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait.
    Houdayer C, Soupre V, Rosenberg-Bourgin M, Martinez H, Tredano M, Feldmann D, Feingold J, Aymard P, Munnich A, Le Bouc Y, Vazquez MP, Bahuau M.
    Ann Genet; 1999 Jul 06; 42(2):69-74. PubMed ID: 10434119
    [Abstract] [Full Text] [Related]

  • 57. Anomalies associated with cleft lip, cleft palate, or both.
    Shprintzen RJ, Siegel-Sadewitz VL, Amato J, Goldberg RB.
    Am J Med Genet; 1985 Apr 06; 20(4):585-95. PubMed ID: 3993684
    [Abstract] [Full Text] [Related]

  • 58. Phenotypic variability in van der Woude syndrome.
    Lacombe D, Pedespan JM, Fontan D, Chateil JF, Verloes A.
    Genet Couns; 1995 Apr 06; 6(3):221-6. PubMed ID: 8588850
    [Abstract] [Full Text] [Related]

  • 59. [Van der Woude syndrome (report of a case)].
    Ergen C, Sayan NB.
    Ankara Univ Hekim Fak Derg; 1985 Apr 06; 12(1):163-9. PubMed ID: 3870090
    [No Abstract] [Full Text] [Related]

  • 60. Congenital lower lip pits (Van der Woude syndrome): report of a case.
    Kirzioglu Z, Ertürk MS.
    J Contemp Dent Pract; 2006 Feb 15; 7(1):134-40. PubMed ID: 16491156
    [Abstract] [Full Text] [Related]

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