These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. [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]
7. [Pedigree of Waardenburg's syndrome in a family]. Kawaguchi Y; Kawa Y; Kawaguchi S; Mizoguchi M; Kubota N Nihon Hifuka Gakkai Zasshi; 1987 Mar; 97(4):437-44. PubMed ID: 3613209 [No Abstract] [Full Text] [Related]
8. [Four families with Waardenburg's syndrome in Shizuoka prefecture (author's transl)]. Tamada A; Kobayashi T Nihon Jibiinkoka Gakkai Kaiho; 1980 Dec; 83(12):1616-9. PubMed ID: 7252625 [No Abstract] [Full Text] [Related]
9. [Waardenburg's syndrome. Report of a family (author's transl)]. Gracia R; Burgueros M; Lledó G; Barrio R; Alvarado F An Esp Pediatr; 1975; 8(4):429-34. PubMed ID: 1147417 [No Abstract] [Full Text] [Related]
10. [Make a diagnosis. Waardenburg's syndrome type 1]. Aksu F Padiatr Padol; 1983; 18(4):399-402. PubMed ID: 6646790 [No Abstract] [Full Text] [Related]
11. [Waardenburg's syndrome. Clinical and genetical study of a family with affected twins]. Carakushansky G; Berthier C AMB Rev Assoc Med Bras; 1975 May; 21(5):159-60. PubMed ID: 1088764 [No Abstract] [Full Text] [Related]
12. Waardenburg syndrome: a report of three cases. Ghosh SK; Bandyopadhyay D; Ghosh A; Biswas SK; Mandal RK Indian J Dermatol Venereol Leprol; 2010; 76(5):550-2. PubMed ID: 20826997 [TBL] [Abstract][Full Text] [Related]
13. [Waardenburg's syndrome. Different clinical manifestations in one family]. Ramalho AS; Arena JF AMB Rev Assoc Med Bras; 1982; 28(9-10):228-9. PubMed ID: 6984961 [No Abstract] [Full Text] [Related]
14. Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene. Badner JA; Chakravarti A Am J Med Genet; 1990 Jan; 35(1):100-4. PubMed ID: 2301458 [TBL] [Abstract][Full Text] [Related]
15. [Waardenburg syndrome type I--autosomal dominant hereditary combination of multiple facial anomalies with cochlear deafness (author's transl)]. Meinecke P Klin Padiatr; 1982 Mar; 194(2):112-6. PubMed ID: 7098370 [TBL] [Abstract][Full Text] [Related]
16. [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; 13(2):125-8. PubMed ID: 5310696 [No Abstract] [Full Text] [Related]