Structure of the Fanconi anaemia monoubiquitin ligase complex | Nature
Fanconi's syndrome induced by a monoclonal Vκ3 light chain in Waldenström's macroglobulinemia - American Journal of Kidney Diseases
Metformin for treatment of cytopenias in children and young adults with Fanconi anemia - ScienceDirect
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure | American Society of Nephrology
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure | American Society of Nephrology
Children | Free Full-Text | Growth Retardation in the Course of Fanconi Syndrome Caused by the 4977-bp Mitochondrial DNA Deletion: A Case Report | HTML
Glycine Amidinotransferase (GATM), Renal Fanconi Syndrome, and Kidney Failure | American Society of Nephrology
Fanconi syndrome-specific biomarkers | Download Table
Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome | NEJM
Fanconi Syndrome: Disease Bioinformatics: Novus Biologicals
The Promise of Tubule Biomarkers in Kidney Disease: A Review - American Journal of Kidney Diseases
Acute Tubular Dysfunction With Fanconi Syndrome: A New Manifestation of Mitochondrial Cytopathies - American Journal of Kidney Diseases
PDF) Adult Idiopathic Renal Fanconi Syndrome: A Case Report
Genes | Free Full-Text | Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences | HTML
MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia - ScienceDirect
MiRNA-200C expression in Fanconi anemia pathway functionally deficient lung cancers | Scientific Reports
Fanconi Syndrome - Renal - Medbullets Step 1
Renal Fanconi Syndrome Is Caused by a Mistargeting-Based Mitochondriopathy - ScienceDirect
Fanconi Syndrome: Disease Bioinformatics: Novus Biologicals
Beyond DNA repair and chromosome instability—Fanconi anaemia as a cellular senescence-associated syndrome | Cell Death & Differentiation
Renal Tubular Defects in Small Animals - Urinary System - Merck Veterinary Manual
Molecular Basis for Autosomal-Dominant Renal Fanconi Syndrome Caused by HNF4A - ScienceDirect
