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Genetic heterogeneity among kindreds with Alport syndromeHASSTEDT, S. J; ATKIN, C. L; SAN JUAN, A. C. JR et al.American journal of human genetics. 1986, Vol 38, Num 6, pp 940-953, issn 0002-9297Article

Fechtner syndrome: clinical and genetic aspectsGERSHONI-BARUCH, R; BARUCH, Y; VIENER, A et al.American journal of medical genetics. 1988, Vol 31, Num 2, pp 357-367, issn 0148-7299Article

Aspects cliniques et génétiques du syndrome d'Alport : Néphrologie = Clinical and genetic aspects of Alport SyndromeGOLSHAYAN, D; VENETZ, J. P; CACHAT, F et al.Revue médicale suisse. 2006, Vol 2, Num 55, pp 593-598, issn 1660-9379, 6 p.Article

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Les néphropathies héréditaires = Hereditary nephritisYOSHIKAWA, N; ITO, H; NAKAMURA, N et al.Pédiatrie (Marseille). 1990, Vol 45, Num 1, pp 5-11, issn 0031-4021Article

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Le lenticône antérieur : aide diagnostique au syndrome d'Alport = Anterior lenticonus: diagnostic aid in Alport syndromeBLAISE, P; DELANAYE, P; MARTALO, O et al.Journal français d'ophtalmologie. 2003, Vol 26, Num 10, pp 1075-1082, issn 0181-5512, 8 p.Article

Néphropathies hématuriques familiales : Maladies rénales héréditaires = Hereditary hematuric nephritis : Hereditary renal disordersGUBLER, M.-C.La Revue du praticien (Paris). 1997, Vol 47, Num 14, pp 1545-1549, issn 0035-2640Article

Complete amino acid sequence of the human α5(IV) collagen chain and identification of a single-base mutation in exon 23 converting glycine 521 in the collagenous domain to cysteine in an alport syndrome patientZHOU, J; HERTZ, J. M; LEINONEN, A et al.The Journal of biological chemistry (Print). 1992, Vol 267, Num 18, pp 12475-12481, issn 0021-9258Article

Ocular manifestations of Alport's syndrome: a case reportACKE, I; PRIEM, H.Bulletin de la Société belge d'ophtalmologie. 1992, Vol 243, pp 123-128, issn 0081-0746Article

Urinary 3-hydroxyproline excretion in Alport's syndrome : a non-invasive screening test ?BARTOSCH, B; VYCUDILIK, W; POPOW, C et al.Archives of disease in childhood. 1991, Vol 66, Num 2, pp 248-251, issn 0003-9888Article

Posttransplant anti-glomerular basement membrane nephritis in related males with Alport syndromeKASHTAN, C. E; BUTKOWSKI, R. J; KLEPPEL, M. M et al.The Journal of laboratory and clinical medicine. 1990, Vol 116, Num 4, pp 508-515, issn 0022-2143Article

Diffuse leiomyomatosis in Alport syndromeCOCHAT, P; GUIBAUD, P; GARCIA TORRES, R et al.The Journal of pediatrics. 1988, Vol 113, Num 2, pp 339-343, issn 0022-3476Article

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Amyloid P component is not present in the glomerular basement membrane in Alport-type hereditary nephritisMELVIN, T; KIM, Y; MICHAEL, A. F et al.The American journal of pathology. 1986, Vol 125, Num 3, pp 460-464, issn 0002-9440Article

Síndrome de Alport: a propósito de um caso = Syndrome de Alport. Observation d'un cas = Alport syndrom. Presentation of one casePAIVA, C. FILHO; RAPOSO, A. FILHO; PAIVA, F et al.Arquivos brasileiros de oftalmologia. 1986, Vol 49, Num 3, pp 86-88, issn 0004-2749Article

Nephritogenic antigen determinants in epidermal and renal basement membranes of kindreds with Alport-type familial nephritisKASHTAN, C; FISH, A. J; KLEPPEL, M et al.The Journal of clinical investigation. 1986, Vol 78, Num 4, pp 1035-1044, issn 0021-9738Article

Advances in Alport syndrome diagnosis using next-generation sequencingARTUSO, Rosangela; FALLERINI, Chiara; LONGO, Ilaria et al.European journal of human genetics. 2012, Vol 20, Num 1, pp 50-57, issn 1018-4813, 8 p.Article

Ocular manifestations and surgical results in patients with Alport syndromeSEYMENOGLU, Göktug; BASER, Esin F.Journal of cataract and refractive surgery. 2009, Vol 35, Num 7, pp 1302-1306, issn 0886-3350, 5 p.Article

Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 geneHERTZ, Jens Michael; PERSSON, Uif; JUNCKER, Inger et al.Human genetics. 2005, Vol 118, Num 1, pp 23-28, issn 0340-6717, 6 p.Article

Alport's syndrome, Goodpasture's syndrome, and type IV collagenHUDSON, Billy G; TRYGGVASON, Karl; SUNDARAMOORTHY, Munirathinam et al.The New England journal of medicine. 2003, Vol 348, Num 25, pp 2543-2556, issn 0028-4793, 14 p.Article