Download Alport Syndrome - A Bibliography and Dictionary for by Philip M. Parker PDF

By Philip M. Parker

In March 2001, the nationwide Institutes of overall healthiness issued the subsequent caution: "The variety of sites providing health-related assets grows on a daily basis. Many websites supply worthwhile details, whereas others could have details that's unreliable or misleading." in addition, as a result of speedy bring up in Internet-based info, many hours should be wasted looking, picking, and printing. on account that purely the smallest fraction of data facing Alport syndrome is listed in se's, equivalent to www.google.com or others, a non-systematic method of web study might be not just time eating, but in addition incomplete. This publication used to be created for doctors, scholars, and contributors of most people who are looking to behavior clinical study utilizing the main complex instruments to be had and spending the smallest amount of time doing so.

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Extra resources for Alport Syndrome - A Bibliography and Dictionary for Physicians, Patients, and Genome Researchers

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Author(s): Kalluri R, van den Heuvel LP, Smeets HJ, Schroder CH, Lemmink HH, Boutaud A, Neilson EG, Hudson BG. Source: Kidney International. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=7783419&query_hl=21&itool=pubmed_docsum • A deletion mutation in the 3' end of the alpha 5(IV) collagen gene in juvenile-onset Alport syndrome. Author(s): Saito A, Sakatsume M, Yamazaki H, Ogata F, Hirasawa Y, Arakawa M. Source: Journal of the American Society of Nephrology : Jasn. 2) detected by fluorescence in situ hybridization in a boy with Alport syndrome.

Db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=10610420&query_hl=21&itool=pubmed_docsum • Cloning of Alport syndrome gene. Author(s): Tryggvason K. Source: Annals of Medicine. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1930913&query_hl=21&itool=pubmed_docsum • COL4A3/COL4A4 mutations: from familial hematuria to autosomal-dominant or recessive Alport syndrome. Author(s): Longo I, Porcedda P, Mari F, Giachino D, Meloni I, Deplano C, Brusco A, Bosio M, Massella L, Lavoratti G, Roccatello D, Frasca G, Mazzucco G, Muda AO, Conti M, Fasciolo F, Arrondel C, Heidet L, Renieri A, De Marchi M.

Source: Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=11773466&query_hl=21&itool=pubmed_docsum • Alport syndrome caused by a 5' deletion within the COL4A5 gene. Author(s): Renieri A, Seri M, Myers JC, Pihlajaniemi T, Sessa A, Rizzoni G, De Marchi M. Source: Human Genetics. db=pubmed&cmd=Retrieve&dopt=A bstractPlus&list_uids=1577459&query_hl=21&itool=pubmed_docsum • Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the Xchromosome comprising exon 9 through 51 of the COL4A5 gene.

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