USE OF A MONOCLONAL ANTIBODY IN DIFFERENTIAL DIAGNOSIS OF CHILDREN WITH HAEMATURIA AND HEREDITARY NEPHRITIS
- 1 June 1986
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 327 (8496) , 1459-1461
- https://doi.org/10.1016/s0140-6736(86)91499-6
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Genetic heterogeneity of Alport syndromeKidney International, 1985
- The clinical spectrum of hereditary nephritisKidney International, 1985
- Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritisKidney International, 1982