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2. Hereditary nephritis, deafness and thrombocytopenia. Case report and review. Thomas HS, Bauer JH. Mo Med; 1984 Jun; 81(6):305-7, 311. PubMed ID: 6377037 [No Abstract] [Full Text] [Related]
3. Macrothrombocytopenia and progressive deafness: a new genetic syndrome. Brodie HA, Chole RA, Griffin GC, White JG. Am J Otol; 1992 Nov; 13(6):507-11. PubMed ID: 1449176 [Abstract] [Full Text] [Related]
4. [Alport's syndrome: hereditary nephropathy with hematuria and deafness]. Giger C, Guignard JP, Pelet B, Campiche M, Krstic R. Rev Med Suisse Romande; 1988 Apr; 108(4):349-55. PubMed ID: 3387770 [No Abstract] [Full Text] [Related]
17. [Chronic hereditary nephropathy with deafness and ocular lesions]. Hauser J. Schweiz Med Wochenschr; 1974 May 18; 104(20):724-8. PubMed ID: 4829630 [No Abstract] [Full Text] [Related]
18. Fechtner syndrome: clinical and genetic aspects. Gershoni-Baruch R, Baruch Y, Viener A, Lichtig C. Am J Med Genet; 1988 Oct 18; 31(2):357-67. PubMed ID: 3232700 [Abstract] [Full Text] [Related]
19. [2 families with Alport's syndrome]. Cohen-Solal J, Delepierre M, Delepierre F, Herrault A. Ann Pediatr (Paris); 1970 Nov 02; 17(11):734-49. PubMed ID: 5484618 [No Abstract] [Full Text] [Related]
20. [Chronic hereditary nephropathy with deafness and eye involvment]. Hauser J. Schweiz Med Wochenschr; 1974 May 25; 104(21):767-72. PubMed ID: 4829025 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]