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61 related items for PubMed ID: 1576755
41. PAX3 mutations and clinical characteristics in Chinese patients with Waardenburg syndrome type 1. Wang J, Li S, Xiao X, Wang P, Guo X, Zhang Q. Mol Vis; 2010 Jun 22; 16():1146-53. PubMed ID: 20664692 [Abstract] [Full Text] [Related]
42. Phenotypic discriminants in the Waardenburg syndrome. Winship I, Beighton P. Clin Genet; 1992 Apr 22; 41(4):181-8. PubMed ID: 1576755 [Abstract] [Full Text] [Related]
43. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Liu XZ, Newton VE, Read AP. Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105 [Abstract] [Full Text] [Related]
45. Waardenburg syndrome in the Turkish deaf population. Silan F, Zafer C, Onder I. Genet Couns; 2006 Jul 02; 17(1):41-8. PubMed ID: 16719276 [Abstract] [Full Text] [Related]
46. Waardenburg's syndrome in Kenyan Africans. Hageman MJ. Trop Geogr Med; 1978 Mar 02; 30(1):45-55. PubMed ID: 675827 [Abstract] [Full Text] [Related]
47. Phenotypic discriminants in the Waardenburg syndrome. Winship I, Beighton P. Clin Genet; 1992 Apr 02; 41(4):181-8. PubMed ID: 1576755 [Abstract] [Full Text] [Related]
48. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Liu XZ, Newton VE, Read AP. Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105 [Abstract] [Full Text] [Related]
50. Waardenburg syndrome in the Turkish deaf population. Silan F, Zafer C, Onder I. Genet Couns; 2006 Jul 02; 17(1):41-8. PubMed ID: 16719276 [Abstract] [Full Text] [Related]
51. Waardenburg's syndrome in Kenyan Africans. Hageman MJ. Trop Geogr Med; 1978 Mar 02; 30(1):45-55. PubMed ID: 675827 [Abstract] [Full Text] [Related]
52. Phenotypic discriminants in the Waardenburg syndrome. Winship I, Beighton P. Clin Genet; 1992 Apr 02; 41(4):181-8. PubMed ID: 1576755 [Abstract] [Full Text] [Related]
53. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Liu XZ, Newton VE, Read AP. Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105 [Abstract] [Full Text] [Related]
54. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC]. Bassabi SK, Medji AP, Doutetien C, Oussa G, Hounkpe YY, Vodouhe SJ, Babagbeto M, Latoundji S. J Fr Ophtalmol; 1997 Jan 02; 20(5):387-90. PubMed ID: 9238477 [Abstract] [Full Text] [Related]
55. [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 Jan 02; 163(2):e85-94. PubMed ID: 22555841 [Abstract] [Full Text] [Related]
56. [Waardenburg's syndrome]. Mouriaux F, Hamedani M, Hurbli T, Uteza Y, Oubaaz A, Morax S. J Fr Ophtalmol; 1999 Jan 02; 22(7):799-809. PubMed ID: 10510766 [No Abstract] [Full Text] [Related]
57. Phenotypic discriminants in the Waardenburg syndrome. Winship I, Beighton P. Clin Genet; 1992 Apr 02; 41(4):181-8. PubMed ID: 1576755 [Abstract] [Full Text] [Related]
58. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Liu XZ, Newton VE, Read AP. Am J Med Genet; 1995 Jan 02; 55(1):95-100. PubMed ID: 7702105 [Abstract] [Full Text] [Related]
59. [A case of Waardenburg-Klein syndrome observed at the Cotonou NUHC]. Bassabi SK, Medji AP, Doutetien C, Oussa G, Hounkpe YY, Vodouhe SJ, Babagbeto M, Latoundji S. J Fr Ophtalmol; 1997 Jan 02; 20(5):387-90. PubMed ID: 9238477 [Abstract] [Full Text] [Related]
60. [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 Jan 02; 163(2):e85-94. PubMed ID: 22555841 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]