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54. [Waardenburg's syndrome associated with unusual facial abnormalities]. Cordier J; Reny A; Stricker M; Brichet B; Raspiller A Rev Otoneuroophtalmol; 1971; 43(4):192-8. PubMed ID: 5113321 [No Abstract] [Full Text] [Related]
55. [Waardenburg-Klein syndrome. Description of 2 cases]. Fregonese B; Vignola G; Mori PG; Grossi Bianchi ML Minerva Pediatr; 1969 Aug; 21(33):1513-9. PubMed ID: 5361984 [No Abstract] [Full Text] [Related]
56. An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome. Baldwin CT; Hoth CF; Amos JA; da-Silva EO; Milunsky A Nature; 1992 Feb; 355(6361):637-8. PubMed ID: 1347149 [TBL] [Abstract][Full Text] [Related]
57. Auditory and vestibular findings in Waardenburg's type II syndrome. Hildesheimer M; Maayan Z; Muchnik C; Rubinstein M; Goodman RM J Laryngol Otol; 1989 Dec; 103(12):1130-3. PubMed ID: 2614228 [TBL] [Abstract][Full Text] [Related]
58. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia]. Amini-Elihou S J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816 [No Abstract] [Full Text] [Related]