Literature DB >> 4951535

Hereditary nephropathy without deafness.

R J Dockhorn.   

Abstract

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Year:  1967        PMID： 4951535     DOI： 10.1001/archpedi.1967.02090230065004

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  2 in total

1.  A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

Authors:  D H Cohn; T Shohat; M Yahav; T Ilan; G Rechavi; L King; M Shohat
Journal:  Am J Hum Genet       Date:  2000-08-04       Impact factor: 11.025

Review 2.  Genetics of Alport's syndrome.

Authors:  J Feingold; E Bois
Journal:  Pediatr Nephrol       Date:  1987-07       Impact factor: 3.714
  2 in total

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