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4. [Diversity of hereditary pathology in the population of Marii El Republic and its differentiation with respect to gene frequencies for hereditary diseases]. Ginter EK; Mamedova RA; Kozlova SI; Galkina VA; Moshkina IS; Rudenskaia GE; Khlebnikova OV; Nurbaev SD; Balanovskaia EV; Rassanov VP Genetika; 1998 Jul; 34(7):963-72. PubMed ID: 9749338 [TBL] [Abstract][Full Text] [Related]
5. [Pedigree analysis of two families with Alport's syndrome]. Wässer S; Theile H; Schöne D; Lemme B Padiatr Grenzgeb; 1980; 19(3):167-71. PubMed ID: 7454376 [No Abstract] [Full Text] [Related]
6. Autosomal dominant Alport's syndrome: study of a large Tunisian family. Kharrat M; Makni S; Makni K; Kammoun K; Charfeddine K; Azaeiz H; Jarraya F; Ben Hmida M; Gubler MC; Ayadi H; Hachicha J Saudi J Kidney Dis Transpl; 2006 Sep; 17(3):320-5. PubMed ID: 16970251 [TBL] [Abstract][Full Text] [Related]
13. Absence of ocular manifestations in autosomal dominant Alport syndrome associated with haematological abnormalties. Colville D; Wang YY; Jamieson R; Collins F; Hood J; Savige J Ophthalmic Genet; 2000 Dec; 21(4):217-25. PubMed ID: 11135492 [TBL] [Abstract][Full Text] [Related]
14. The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms. Liu J; Colville D; Wang YY; Baird PN; Guymer RH; Savige J Br J Ophthalmol; 2009 Mar; 93(3):379-82. PubMed ID: 19019939 [TBL] [Abstract][Full Text] [Related]
15. Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype. Ars E; Tazón-Vega B; Ruiz P; Nogués C; Arnedo N; Rajmil O; Torra R Eur J Hum Genet; 2005 Sep; 13(9):1040-6. PubMed ID: 15957001 [TBL] [Abstract][Full Text] [Related]
16. Spectrum of clinical features and type IV collagen alpha-chain distribution in Chinese patients with Alport syndrome. Wei G; Zhihong L; Huiping C; Caihong Z; Zhaohong C; Leishi L Nephrol Dial Transplant; 2006 Nov; 21(11):3146-54. PubMed ID: 16940319 [TBL] [Abstract][Full Text] [Related]
17. [The first experience in Russia of using DNA diagnosis in Alport's syndrome in a family with a unique morphological picture of the kidney lesion]. Tsalikova FD; Ignatova MS; Krasnopol'skaia KD; Tverskaia SM; Brydun AV Ter Arkh; 1995; 67(4):45-7. PubMed ID: 7784975 [TBL] [Abstract][Full Text] [Related]
18. [Alport syndrome in the light of current molecular genetics]. Pirson Y Bull Mem Acad R Med Belg; 1996; 151(10-11):447-52; discussion 452-3. PubMed ID: 9491622 [TBL] [Abstract][Full Text] [Related]