Pages that link to "Q71070681"
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The following pages link to Renal pathology of fetuses with congenital nephrotic syndrome of the Finnish type. A qualitative and quantitative light microscopic study (Q71070681):
Displaying 8 items.
- Minimal change disease and idiopathic FSGS: manifestations of the same disease. (Q38982416) (← links)
- Introduction: Review of microscopic studies on the fetal and neonatal kidney (Q41645460) (← links)
- Role of nephrin in cell junction formation in human nephrogenesis (Q41778709) (← links)
- Nephrosis and disturbances of neuronal migration in male siblings--a new hereditary disorder? (Q41790709) (← links)
- Glycosaminoglycans in urine and amniotic fluid in congenital nephrotic syndrome of the Finnish type (Q50769061) (← links)
- No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations. (Q53886868) (← links)
- Histological features of glomerular immaturity in infants and small children with normal or altered tubular function (Q70807110) (← links)
- Prenatal diagnosis of congenital nephrosis of the Finnish type (CNF) in the second trimester (Q72081886) (← links)