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Journal Abstract Search

157 related items for PubMed ID: 519896

  • 21. The Peters' plus syndrome: a review.
    Maillette de Buy Wenniger-Prick LJ, Hennekam RC.
    Ann Genet; 2002; 45(2):97-103. PubMed ID: 12119218
    [Abstract] [Full Text] [Related]

  • 22. Ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome. Its association with conductive hearing loss.
    Robinson GC, Wildervanck LS, Chiang TP.
    J Pediatr; 1973 Jan; 82(1):107-9. PubMed ID: 4681851
    [No Abstract] [Full Text] [Related]

  • 23. Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.
    Stevenson RE, May M, Arena JF, Millar EA, Scott CI, Schroer RJ, Simensen RJ, Lubs HA, Schwartz CE.
    Am J Med Genet; 1994 Sep 01; 52(3):339-45. PubMed ID: 7810566
    [Abstract] [Full Text] [Related]

  • 24. Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
    Váradi V, Szabó L, Papp Z.
    J Med Genet; 1980 Apr 01; 17(2):119-22. PubMed ID: 7381865
    [Abstract] [Full Text] [Related]

  • 25. A familial tetraphocomelia syndrome involving limb deformities, cleft lip, cleft palate, and associated anomalies--a new syndrome.
    Kucheria K, Bhargava SK, Bamezai R, Bhutani P.
    Hum Genet; 1976 Aug 30; 33(3):323-6. PubMed ID: 964992
    [Abstract] [Full Text] [Related]

  • 26. The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).
    Porteous ME, Curtis A, Lindsay S, Williams O, Goudie D, Kamakari S, Bhattacharya SS.
    Genomics; 1992 Oct 30; 14(2):298-301. PubMed ID: 1427846
    [Abstract] [Full Text] [Related]

  • 27. The EEC syndrome. Report of six patients.
    Pashayan HM, Pruzansky S, Solomon L.
    Birth Defects Orig Artic Ser; 1974 Oct 30; 10(7):105-27. PubMed ID: 4425508
    [No Abstract] [Full Text] [Related]

  • 28. Robin sequence with facial and digital anomalies in two half-brothers by the same mother.
    Chitayat D, Meunier CM, Hodgkinson KA, Azouz ME.
    Am J Med Genet; 1991 Aug 01; 40(2):167-72. PubMed ID: 1897570
    [Abstract] [Full Text] [Related]

  • 29. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F.
    Am J Med Genet; 1983 May 01; 15(1):135-40. PubMed ID: 6859112
    [Abstract] [Full Text] [Related]

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  • 31. [Ectrodactyly, ectodermal dysplasia, cleft lip and palate syndrome (EEC syndrome)].
    Ostorharics-Horváth G, Lázár I.
    Orv Hetil; 1989 Oct 08; 130(41):2211-2. PubMed ID: 2812754
    [Abstract] [Full Text] [Related]

  • 32.
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  • 33. Child with fronto-facio-nasal dysplasia, Hirschsprung's disease and hypospadias.
    Fryer AE.
    Clin Dysmorphol; 1993 Apr 08; 2(2):120-2. PubMed ID: 8281272
    [Abstract] [Full Text] [Related]

  • 34. EEC syndrome without ectrodactyly? Report of 8 cases.
    Küster W, Majewski F, Meinecke P.
    Clin Genet; 1985 Aug 08; 28(2):130-5. PubMed ID: 4042394
    [Abstract] [Full Text] [Related]

  • 35.
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  • 36. [The risk of reappearance of a harelip-cleft palate or other congenital anomalies (congenital hip dislocation, cutaneous syndactyly) in a family].
    Klein D.
    J Genet Hum; 1971 Sep 08; 19(3):267-9. PubMed ID: 5150018
    [No Abstract] [Full Text] [Related]

  • 37. Deletion of the short arm of chromosome No. 10.
    Shokeir MH, Ray M, Hamerton JL, Bauder F, O'Brien H.
    J Med Genet; 1975 Mar 08; 12(1):99-103. PubMed ID: 47396
    [Abstract] [Full Text] [Related]

  • 38. Expressivity of heritable telecanthus in five generations of a kindred.
    Juberg RC, Hirsch R.
    Am J Hum Genet; 1971 Nov 08; 23(6):547-54. PubMed ID: 5002294
    [No Abstract] [Full Text] [Related]

  • 39. Association and Mutation Analyses of the IRF6 Gene in Families With Nonsyndromic and Syndromic Cleft Lip and/or Cleft Palate.
    Pegelow M, Koillinen H, Magnusson M, Fransson I, Unneberg P, Kere J, Karsten A, Peyrard-Janvid M.
    Cleft Palate Craniofac J; 2014 Jan 08; 51(1):49-55. PubMed ID: 23394314
    [Abstract] [Full Text] [Related]

  • 40.
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