These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
8. Genetic aspects of renal disease: a survey of the various recognized forms. Platt M Clin Pediatr (Phila); 1976 Nov; 15(11):1024-8. PubMed ID: 184999 [No Abstract] [Full Text] [Related]
9. Hereditary disorders of the kidney. II. Hereditary nephropathies. Kissane JM Perspect Pediatr Pathol; 1973; 1():147-87. PubMed ID: 4596311 [No Abstract] [Full Text] [Related]
11. Idiopathic low molecular weight proteinuria associated with hypercalciuric nephrocalcinosis in Japanese children is due to mutations of the renal chloride channel (CLCN5). Lloyd SE; Pearce SH; Günther W; Kawaguchi H; Igarashi T; Jentsch TJ; Thakker RV J Clin Invest; 1997 Mar; 99(5):967-74. PubMed ID: 9062355 [TBL] [Abstract][Full Text] [Related]
12. [Contribution of molecular biology to the study of renal tubular diseases]. Rodríguez Soriano J An Esp Pediatr; 1997 Jun; Spec No 1():40-2. PubMed ID: 9382265 [No Abstract] [Full Text] [Related]