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61 related items for PubMed ID: 1576755
21. Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindred. Dow E, Cross S, Wolgemuth DJ, Lyonnet S, Mulligan LM, Mascari M, Ladda R, Williamson R. Am J Med Genet; 1994 Oct 15; 53(1):75-80. PubMed ID: 7802041 [Abstract] [Full Text] [Related]
27. [Klein-Waardenburg syndrome. Report of 3 cases in a family with a review of the literature]. Piechowiak H, Wasmer C, Göbel FD. Laryngol Rhinol Otol (Stuttg); 1985 Apr 15; 64(4):194-7. PubMed ID: 4010406 [Abstract] [Full Text] [Related]
28. A homozygous mutation in the endothelin-3 gene associated with a combined Waardenburg type 2 and Hirschsprung phenotype (Shah-Waardenburg syndrome). Hofstra RM, Osinga J, Tan-Sindhunata G, Wu Y, Kamsteeg EJ, Stulp RP, van Ravenswaaij-Arts C, Majoor-Krakauer D, Angrist M, Chakravarti A, Meijers C, Buys CH. Nat Genet; 1996 Apr 15; 12(4):445-7. PubMed ID: 8630503 [Abstract] [Full Text] [Related]
36. [Hearing disorders in Waardenburg's syndrome]. Schulze W, Ganz H. HNO; 1972 Jul 15; 20(7):203-7. PubMed ID: 5071320 [No Abstract] [Full Text] [Related]
37. Hearing impairment and pigmentary disturbance. Beighton P, Ramesar R, Winship I, Viljoen D, Greenberg J, Young K, Curtis D, Sellars S. Ann N Y Acad Sci; 1991 Jul 15; 630():152-66. PubMed ID: 1952586 [Abstract] [Full Text] [Related]
38. Waardenburg syndrome in South Africa. Part I. An evaluation of the clinical findings in 11 families. de Saxe M, Kromberg JG, Jenkins T. S Afr Med J; 1984 Aug 18; 66(7):256-61. PubMed ID: 6463802 [Abstract] [Full Text] [Related]