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Journal Abstract Search

155 related items for PubMed ID: 728559

  • 1. The facio-genito-popliteal syndrome.
    Escobar V, Weaver DD.
    Birth Defects Orig Artic Ser; 1978; 14(6B):185-92. PubMed ID: 728559
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
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  • 3. Popliteal pterygium syndrome: a phenotypic and genetic analysis.
    Escobar V, Weaver D.
    J Med Genet; 1978 Feb; 15(1):35-42. PubMed ID: 633318
    [Abstract] [Full Text] [Related]

  • 4.
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  • 5. [Van der Woude's syndrome].
    Nungaray M, Fragoso R, Hernández A, Rivas F, Cantú JM.
    Bol Med Hosp Infant Mex; 1980 Feb; 37(1):131-6. PubMed ID: 7352961
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. [Popliteal pterygium syndrome. A exceptional case].
    Brun MF, Delcampe P, Retout A, Bachy B, Peron JM.
    Rev Stomatol Chir Maxillofac; 1994 Feb; 95(5):343-7. PubMed ID: 7984954
    [Abstract] [Full Text] [Related]

  • 8. The popliteal pterygium syndrome: distinct phenotypic variation in two families.
    Hammer J, Kläusler M, Schinzel A.
    Helv Paediatr Acta; 1989 Jun; 43(5-6):507-14. PubMed ID: 2745146
    [Abstract] [Full Text] [Related]

  • 9. A case of facio-genito-popliteal syndrome.
    Hamamoto J, Matsumoto T.
    Ann Plast Surg; 1984 Sep; 13(3):224-9. PubMed ID: 6093671
    [Abstract] [Full Text] [Related]

  • 10. Popliteal pterygium syndrome in monozygous twins.
    Bixler D, Poland C, Nance WE.
    Birth Defects Orig Artic Ser; 1974 Sep; 10(5):167-75. PubMed ID: 4469980
    [No Abstract] [Full Text] [Related]

  • 11. [Knee pterygium syndrome in a newborn infant].
    Meinecke P, Menzel J, Froster-Iskenius U.
    Monatsschr Kinderheilkd; 1989 Apr; 137(4):228-30. PubMed ID: 2543917
    [Abstract] [Full Text] [Related]

  • 12. [Van-der-Woude Syndrome].
    Del Frari B, Amort M, Janecke AR, Schutte BC, Piza-Katzer H.
    Klin Padiatr; 2008 Apr; 220(1):26-8. PubMed ID: 18095255
    [Abstract] [Full Text] [Related]

  • 13. [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
    [No Abstract] [Full Text] [Related]

  • 14. [Genetic analysis of two families with van der Woude's syndrome (lip pits, cleft palate, and cleft lip syndrome)].
    Burdick AB, Ma LA, Gao N, Dai ZH.
    Yi Chuan Xue Bao; 1988 Apr; 15(5):396-400. PubMed ID: 3273683
    [No Abstract] [Full Text] [Related]

  • 15. Bartsocas-Papas syndrome with variable expressivity in an Egyptian family.
    Zaki MS, Kamel AK, Effat LK, El-Ruby MO.
    Genet Couns; 2012 Apr; 23(2):269-79. PubMed ID: 22876587
    [Abstract] [Full Text] [Related]

  • 16. 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
    [Abstract] [Full Text] [Related]

  • 17. [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 24; 117(4):127-34. PubMed ID: 3823824
    [Abstract] [Full Text] [Related]

  • 18. Oral adhesions associated with cleft lip and palate and lip fistulae.
    Shaw WC, Simpson JP.
    Cleft Palate J; 1980 Apr 24; 17(2):127-31. PubMed ID: 6929230
    [Abstract] [Full Text] [Related]

  • 19. [Heredity and empirical hereditary prognosis of cleft lip and palate in 326 cases out of 309 unselected Swiss families].
    Hanhart E, Kälin A.
    J Genet Hum; 1972 Jun 24; 20(2):93-134. PubMed ID: 4660640
    [No Abstract] [Full Text] [Related]

  • 20. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug 24; 12(4):377-409. PubMed ID: 7124793
    [Abstract] [Full Text] [Related]

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