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Journal Abstract Search

302 related items for PubMed ID: 16719276

  • 21. [Waardenburg's syndrome and severe cyanotic cardiopathy].
    Mathieu M, Bourges E, Caron F, Piussan C.
    Arch Fr Pediatr; 1990 Nov; 47(9):657-9. PubMed ID: 2078126
    [Abstract] [Full Text] [Related]

  • 22. Waardenburg syndrome Type II.
    Singh I, Maharjan M, Gautam DK, Mehar R, Gathwala G.
    Kathmandu Univ Med J (KUMJ); 2006 Nov; 4(4):506-9. PubMed ID: 18603964
    [Abstract] [Full Text] [Related]

  • 23. [Waardenburg syndrome. Report of a familial case].
    Khaldi F, Serbegi M, Mokadem H, Lazzem B, Bennaceur B.
    Ann Pediatr (Paris); 1990 Jan; 37(1):55-8. PubMed ID: 2316963
    [Abstract] [Full Text] [Related]

  • 24. [Atypical manifestations in familial type 1 Waardenburg syndrome].
    Sans B, Calvas P, Bazex J.
    Ann Dermatol Venereol; 1998 Jan; 125(1):37-41. PubMed ID: 9747206
    [Abstract] [Full Text] [Related]

  • 25. Type II Waardenburg syndrome.
    Varughese S, Kumar A, Rao S, Puliyel JM.
    Indian Pediatr; 1988 Apr; 25(4):384-6. PubMed ID: 3225049
    [No Abstract] [Full Text] [Related]

  • 26. Genetic heterogeneity in the Waardenburg syndrome.
    Arias S.
    Birth Defects Orig Artic Ser; 1971 Mar; 07(4):87-101. PubMed ID: 5006208
    [Abstract] [Full Text] [Related]

  • 27. The association of Waardenburg syndrome and Hirschsprung megacolon.
    Omenn GS, McKusick VA.
    Am J Med Genet; 1979 Mar; 3(3):217-23. PubMed ID: 484594
    [Abstract] [Full Text] [Related]

  • 28. Waardenburg syndrome with extended aganglionosis: report of 3 new cases.
    Karaca I, Turk E, Ortac R, Kandirici A.
    J Pediatr Surg; 2009 Jun; 44(6):E9-13. PubMed ID: 19524716
    [Abstract] [Full Text] [Related]

  • 29. [Waardenburg's syndrome].
    Gimñenez F, Carbonell R, Pérez F, Lozano I.
    An Otorrinolaringol Ibero Am; 1994 Jun; 21(4):425-32. PubMed ID: 8092450
    [Abstract] [Full Text] [Related]

  • 30. [Waardenburg syndrome].
    Veres G, Kárpáti S, Karászi V, Czenthe Z, Horváth A.
    Orv Hetil; 2004 Jul 18; 145(29):1523-6. PubMed ID: 15453024
    [Abstract] [Full Text] [Related]

  • 31. Child neurology: a patient with dissimilar eye color and deafness.
    Soni CR, Kumar G.
    Neurology; 2010 Feb 23; 74(8):e25-6. PubMed ID: 20177114
    [No Abstract] [Full Text] [Related]

  • 32. Waardenburg syndrome type I in a child with deletion (2) (q35q36.2).
    Kirkpatrick SJ, Kent CM, Laxova R, Sekhon GS.
    Am J Med Genet; 1992 Nov 15; 44(5):699-700. PubMed ID: 1481835
    [No Abstract] [Full Text] [Related]

  • 33. [Waardenburg syndrome and Hirschsprung disease].
    Vázquez Rueda F, Blesa Sánchez E, Núñez Núñez R, Galán Gómez E.
    An Esp Pediatr; 1998 Mar 15; 48(3):306-8. PubMed ID: 9608095
    [No Abstract] [Full Text] [Related]

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  • 35. [Waardenburg Syndrome: a review of literature and case reports].
    Salvatore S, Carnevale C, Infussi R, Arrico L, Mafrici M, Plateroti AM, Vingolo EM.
    Clin Ter; 2012 Mar 15; 163(2):e85-94. PubMed ID: 22555841
    [Abstract] [Full Text] [Related]

  • 36. Molecular heterogeneity in two families with auditory pigmentary syndromes: the role of neuroimaging and genetic analysis in deafness.
    Shears D, Conlon H, Murakami T, Fukai K, Alles R, Trembath R, Bitner-Glindzicz M.
    Clin Genet; 2004 May 15; 65(5):384-9. PubMed ID: 15099345
    [Abstract] [Full Text] [Related]

  • 37. Mental retardation and EEG abnormalities in Waardenburg's syndrome: two case reports (EEG anomalies in Waardenburg's syndrome).
    Cantani A, Bamonte G, Tacconi ML.
    Padiatr Padol; 1989 May 15; 24(2):137-40. PubMed ID: 2503803
    [Abstract] [Full Text] [Related]

  • 38. [Waardenburg's syndrome. A familial case relating to 4 generations and 23 individuals].
    Roux C, Baheux G, Gaulier M, Caldera R, Soepardan L.
    Ann Genet; 1970 Jun 15; 13(2):125-8. PubMed ID: 5310696
    [No Abstract] [Full Text] [Related]

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