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Journal Abstract Search

251 related items for PubMed ID: 3460725

  • 21.
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  • 23. Clinical and genetic features of Van der Woude syndrome in two large families in Brazil.
    Martelli-Junior H, Chaves MR, Swerts MS, de Miranda RT, Bonan PR, Coletta RD.
    Cleft Palate Craniofac J; 2007 May; 44(3):239-43. PubMed ID: 17477759
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  • 24. 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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  • 25. 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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  • 26. [Genetic characteristics of the "EEC" syndrome (ectrodactyly, ectodermal dysplasis, cheilognathopalatoschisis)].
    Lur'e IV, Laziuk GI, Usova IuI.
    Genetika; 1976 Jan; 12(7):125-31. PubMed ID: 1001885
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  • 27. A case of facio-genito-popliteal syndrome.
    Hamamoto J, Matsumoto T.
    Ann Plast Surg; 1984 Sep; 13(3):224-9. PubMed ID: 6093671
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  • 28. Variable expression of the popliteal pterygium syndrome in two 3-generation families.
    Soekarman D, Cobben JM, Vogels A, Spauwen PH, Fryns JP.
    Clin Genet; 1995 Apr; 47(4):169-74. PubMed ID: 7628117
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  • 31. Phenotypic overlap of the BBB and G syndromes.
    Cordero JF, Holmes LB.
    Am J Med Genet; 1978 Apr; 2(2):145-52. PubMed ID: 263434
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  • 32. [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 Apr; 20(4):200-4. PubMed ID: 20626329
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  • 33. 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 Apr; 5(2):117-23. PubMed ID: 7395906
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  • 34. [The popliteal pterygium syndrome. A dominant autosomal malformation syndrome].
    Pfeiffer RA, Tünte W, Reinken M.
    Z Kinderheilkd; 1970 Apr; 108(2):103-16. PubMed ID: 4325529
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  • 35. Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.
    Peyrard-Janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, Hukki J, Larson O, Karsten AL, Kere J.
    Eur J Hum Genet; 2005 Dec; 13(12):1261-7. PubMed ID: 16160700
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  • 36. Van der Woude syndrome: clinical presentation in 64 patients.
    Huang JJ, Hou JW, Tan YC, Chen KT, Lo LJ, Chen YR.
    Cleft Palate Craniofac J; 2007 Nov; 44(6):649-52. PubMed ID: 18177185
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